Information on the Admixed - U.S. Caucasian American Metapopulation
The U.S. Caucasian American Metapopulation (Admixed - U.S. Caucasian American) consists of 12,657 haplotypes (at least minimal) which
were published in 9 population studies and
were additionally submitted via personal communication (6 submissions)
.
Metapopulation substrcuture
Most common haplotypes
Count |
DYS19 |
DYS389I |
DYS389II |
DYS390 |
DYS391 |
DYS392 |
DYS393 |
DYS385 |
634 |
14 |
13 |
29 |
24 |
11 |
13 |
13 |
11,14 |
354 |
14 |
13 |
29 |
23 |
11 |
13 |
13 |
11,14 |
286 |
14 |
13 |
29 |
24 |
10 |
13 |
13 |
11,14 |
196 |
14 |
13 |
29 |
24 |
11 |
13 |
13 |
11,15 |
172 |
14 |
12 |
28 |
22 |
10 |
11 |
13 |
13,14 |
148 |
14 |
13 |
30 |
24 |
11 |
13 |
13 |
11,14 |
146 |
14 |
14 |
30 |
24 |
11 |
13 |
13 |
11,14 |
129 |
14 |
13 |
29 |
25 |
11 |
14 |
13 |
11,13 |
123 |
14 |
13 |
29 |
24 |
10 |
13 |
13 |
11,15 |
119 |
14 |
13 |
30 |
24 |
10 |
13 |
13 |
11,14 |
Count |
DYS391 |
DYS389I |
DYS439 |
DYS389II |
DYS438 |
DYS437 |
DYS19 |
DYS392 |
DYS393 |
DYS390 |
DYS385 |
232 |
11 |
13 |
12 |
29 |
12 |
15 |
14 |
13 |
13 |
24 |
11,14 |
153 |
11 |
13 |
12 |
29 |
12 |
15 |
14 |
13 |
13 |
23 |
11,14 |
115 |
10 |
12 |
11 |
28 |
10 |
16 |
14 |
11 |
13 |
22 |
13,14 |
114 |
10 |
13 |
12 |
29 |
12 |
15 |
14 |
13 |
13 |
24 |
11,14 |
112 |
11 |
13 |
11 |
29 |
12 |
15 |
14 |
13 |
13 |
24 |
11,14 |
80 |
11 |
13 |
12 |
29 |
12 |
15 |
14 |
14 |
13 |
25 |
11,13 |
71 |
11 |
13 |
12 |
29 |
12 |
15 |
14 |
13 |
13 |
24 |
11,15 |
69 |
11 |
13 |
11 |
29 |
12 |
15 |
14 |
13 |
13 |
23 |
11,14 |
66 |
11 |
13 |
12 |
30 |
12 |
15 |
14 |
13 |
13 |
24 |
11,14 |
65 |
10 |
13 |
12 |
29 |
12 |
15 |
14 |
13 |
13 |
23 |
11,14 |
Count |
DYS456 |
DYS389I |
DYS390 |
DYS389II |
DYS458 |
DYS19 |
DYS385 |
DYS393 |
DYS391 |
DYS439 |
DYS635 |
DYS392 |
YGATAH4 |
DYS437 |
DYS438 |
DYS448 |
24 |
16 |
13 |
24 |
29 |
17 |
14 |
11,14 |
13 |
11 |
12 |
23 |
13 |
12 |
15 |
12 |
19 |
17 |
16 |
13 |
24 |
29 |
17 |
14 |
11,14 |
13 |
10 |
12 |
23 |
13 |
12 |
15 |
12 |
19 |
17 |
17 |
13 |
25 |
29 |
17 |
14 |
11,13 |
13 |
11 |
12 |
23 |
14 |
12 |
15 |
12 |
18 |
16 |
15 |
13 |
24 |
29 |
17 |
14 |
11,14 |
13 |
11 |
12 |
23 |
13 |
12 |
15 |
12 |
19 |
15 |
16 |
13 |
24 |
29 |
16 |
14 |
11,14 |
13 |
11 |
12 |
23 |
13 |
12 |
15 |
12 |
19 |
13 |
15 |
13 |
24 |
29 |
17 |
14 |
11,14 |
13 |
11 |
11 |
23 |
13 |
12 |
15 |
12 |
19 |
12 |
15 |
12 |
22 |
28 |
15 |
14 |
13,14 |
13 |
10 |
11 |
21 |
11 |
11 |
16 |
10 |
20 |
11 |
16 |
13 |
24 |
29 |
18 |
14 |
11,14 |
13 |
11 |
12 |
23 |
13 |
12 |
15 |
12 |
19 |
11 |
16 |
13 |
25 |
29 |
17 |
14 |
11,13 |
13 |
11 |
12 |
23 |
14 |
12 |
15 |
12 |
18 |
10 |
15 |
13 |
24 |
30 |
18 |
14 |
11,14 |
13 |
10 |
12 |
24 |
13 |
13 |
15 |
12 |
19 |
Count |
DYS576 |
DYS389I |
DYS448 |
DYS389II |
DYS19 |
DYS391 |
DYS481 |
DYS549 |
DYS533 |
DYS438 |
DYS437 |
DYS570 |
DYS635 |
DYS390 |
DYS439 |
DYS392 |
DYS643 |
DYS393 |
DYS458 |
DYS385 |
DYS456 |
YGATAH4 |
3 |
17 |
13 |
19 |
29 |
14 |
11 |
22 |
13 |
12 |
12 |
14 |
17 |
23 |
24 |
12 |
13 |
10 |
13 |
16 |
12,14 |
16 |
12 |
3 |
17 |
13 |
19 |
29 |
14 |
11 |
22 |
13 |
12 |
12 |
15 |
17 |
23 |
23 |
12 |
13 |
10 |
13 |
16 |
11,14 |
15 |
12 |
3 |
18 |
13 |
20 |
29 |
16 |
10 |
25 |
12 |
12 |
11 |
14 |
19 |
23 |
25 |
11 |
11 |
10 |
13 |
16 |
11,14 |
17 |
12 |
3 |
19 |
13 |
19 |
30 |
14 |
11 |
23 |
13 |
13 |
12 |
15 |
17 |
23 |
25 |
12 |
13 |
10 |
13 |
17 |
11,14 |
14 |
11 |
2 |
14 |
12 |
21 |
29 |
14 |
10 |
22 |
13 |
9 |
10 |
16 |
18 |
23 |
22 |
11 |
11 |
12 |
12 |
17 |
13,14 |
15 |
12 |
2 |
14 |
14 |
20 |
31 |
15 |
10 |
21 |
12 |
12 |
9 |
14 |
17 |
22 |
23 |
12 |
13 |
10 |
13 |
17 |
13,17 |
16 |
12 |
2 |
15 |
12 |
20 |
28 |
14 |
11 |
25 |
12 |
11 |
10 |
16 |
19 |
22 |
23 |
11 |
11 |
12 |
13 |
15 |
13,15 |
14 |
11 |
2 |
15 |
12 |
21 |
31 |
15 |
10 |
20 |
12 |
9 |
10 |
16 |
19 |
20 |
22 |
11 |
11 |
11 |
14 |
16 |
14,15 |
15 |
12 |
2 |
15 |
12 |
23 |
28 |
15 |
10 |
21 |
12 |
10 |
10 |
15 |
17 |
21 |
21 |
11 |
11 |
12 |
14 |
16 |
14,15 |
17 |
11 |
2 |
15 |
13 |
20 |
30 |
13 |
11 |
26 |
13 |
11 |
11 |
14 |
19 |
22 |
24 |
12 |
16 |
10 |
13 |
16 |
15,17 |
16 |
11 |
Count |
DYS576 |
DYS389I |
DYS635 |
DYS389II |
DYS627 |
DYS460 |
DYS458 |
DYS19 |
YGATAH4 |
DYS448 |
DYS391 |
DYS456 |
DYS390 |
DYS438 |
DYS392 |
DYS518 |
DYS570 |
DYS437 |
DYS385 |
DYS449 |
DYS393 |
DYS439 |
DYS481 |
DYF387S1 |
DYS533 |
3 |
16 |
13 |
21 |
30 |
20 |
10 |
18 |
15 |
11 |
19 |
10 |
15 |
23 |
9 |
13 |
36 |
18 |
14 |
14,16 |
33 |
13 |
11 |
22 |
38,38 |
12 |
3 |
16 |
13 |
23 |
29 |
21 |
11 |
17 |
14 |
12 |
19 |
11 |
15 |
23 |
12 |
13 |
36 |
17 |
15 |
12,14 |
31 |
12 |
12 |
22 |
35,36 |
12 |
2 |
15 |
12 |
21 |
28 |
21 |
10 |
16 |
15 |
11 |
23 |
10 |
17 |
21 |
10 |
11 |
37 |
17 |
15 |
14,15 |
31 |
14 |
11 |
21 |
37,38 |
10 |
2 |
16 |
13 |
23 |
29 |
23 |
11 |
17 |
14 |
12 |
19 |
11 |
16 |
23 |
12 |
13 |
38 |
17 |
15 |
11,14 |
29 |
14 |
12 |
22 |
35,37 |
12 |
2 |
16 |
13 |
23 |
30 |
21 |
9 |
15 |
13 |
12 |
20 |
10 |
15 |
24 |
10 |
11 |
41 |
20 |
14 |
16,18 |
32 |
13 |
12 |
22 |
35,37 |
12 |
2 |
17 |
13 |
23 |
29 |
18 |
11 |
17 |
14 |
12 |
19 |
11 |
16 |
24 |
12 |
13 |
37 |
17 |
15 |
11,14 |
30 |
14 |
12 |
22 |
35,36 |
12 |
2 |
17 |
13 |
23 |
29 |
21 |
10 |
16 |
14 |
12 |
19 |
11 |
15 |
24 |
12 |
13 |
40 |
17 |
14 |
9,14 |
30 |
13 |
12 |
22 |
35,36 |
12 |
2 |
17 |
13 |
23 |
29 |
22 |
10 |
18 |
14 |
11 |
19 |
10 |
16 |
24 |
12 |
13 |
38 |
18 |
15 |
12,15 |
29 |
13 |
12 |
22 |
35,36 |
13 |
2 |
17 |
13 |
23 |
29 |
24 |
11 |
16 |
14 |
12 |
19 |
11 |
16 |
24 |
12 |
13 |
37 |
17 |
14 |
12,14 |
29 |
13 |
12 |
22 |
35,36 |
12 |
2 |
17 |
13 |
23 |
30 |
20 |
11 |
16 |
14 |
11 |
19 |
11 |
15 |
24 |
12 |
13 |
39 |
17 |
15 |
11,15 |
30 |
13 |
12 |
22 |
35,36 |
12 |
Count |
DYS19 |
DYS389I |
DYS389II |
DYS390 |
DYS391 |
DYS392 |
DYS393 |
DYS385 |
DYS439 |
DYS438 |
DYS437 |
DYS456 |
DYS458 |
DYS635 |
YGATAH4 |
DYS448 |
DYS576 |
DYS481 |
DYS549 |
DYS533 |
DYS570 |
DYS643 |
DYS627 |
DYS460 |
DYS518 |
DYS449 |
DYF387S1 |
2 |
13 |
13 |
29 |
25 |
11 |
13 |
13 |
11,14 |
13 |
12 |
15 |
18 |
16 |
23 |
12 |
19 |
19 |
22 |
13 |
12 |
17 |
10 |
24 |
11 |
39 |
29 |
35,36 |
2 |
13 |
13 |
30 |
24 |
10 |
11 |
13 |
16,18 |
12 |
10 |
14 |
15 |
15 |
23 |
12 |
20 |
16 |
22 |
12 |
12 |
20 |
14 |
21 |
9 |
41 |
32 |
35,37 |
2 |
14 |
12 |
28 |
25 |
10 |
13 |
13 |
11,14 |
12 |
12 |
15 |
16 |
18 |
23 |
11 |
19 |
18 |
22 |
14 |
12 |
17 |
10 |
22 |
10 |
38 |
31 |
35,37 |
2 |
14 |
13 |
29 |
23 |
11 |
13 |
13 |
11,14 |
13 |
12 |
15 |
15 |
17 |
24 |
12 |
19 |
18 |
22 |
13 |
12 |
17 |
11 |
22 |
11 |
36 |
30 |
35,36 |
2 |
14 |
13 |
29 |
24 |
10 |
13 |
13 |
11,14 |
12 |
12 |
15 |
16 |
17 |
23 |
12 |
19 |
19 |
22 |
13 |
12 |
17 |
10 |
25 |
11 |
39 |
29 |
35,37 |
2 |
14 |
13 |
29 |
24 |
10 |
13 |
13 |
12,15 |
12 |
12 |
15 |
16 |
18 |
23 |
11 |
19 |
17 |
22 |
14 |
13 |
18 |
10 |
22 |
10 |
38 |
29 |
35,36 |
2 |
14 |
13 |
29 |
24 |
11 |
13 |
12 |
12,14 |
11 |
12 |
15 |
15 |
17 |
24 |
12 |
19 |
18 |
19 |
13 |
12 |
17 |
10 |
22 |
11 |
39 |
33 |
35,36 |
2 |
14 |
13 |
29 |
24 |
11 |
13 |
13 |
12,14 |
12 |
12 |
14 |
16 |
16 |
23 |
12 |
19 |
17 |
22 |
13 |
12 |
17 |
10 |
24 |
11 |
37 |
29 |
35,36 |
2 |
14 |
13 |
29 |
25 |
11 |
13 |
13 |
11,14 |
13 |
12 |
16 |
17 |
17 |
23 |
12 |
19 |
18 |
22 |
12 |
12 |
17 |
10 |
23 |
11 |
38 |
30 |
35,37 |
2 |
14 |
13 |
29 |
25 |
12 |
13 |
12 |
11,14 |
12 |
13 |
15 |
17 |
18 |
23 |
12 |
20 |
19 |
23 |
13 |
12 |
17 |
10 |
22 |
11 |
37 |
29 |
35,37 |
Discrete-Laplace frequency estimation (Minimal)
- Release
- R69
- Loci included
- DYS19, DYS389I, DYS389II*, DYS390, DYS391, DYS392, DYS393
- Central haplotypes
- 49
- EM converged
- true
- EM iterations
- 89
- GLM method
- internal_coef
- Init method
- pam
- Threshold frequency
- 1 in 287,020
- Per locus details
- DL centers distribution (download PDF)
Table of haplotype centers (click to show/hide)
|
DYS19 |
DYS389I |
DYS389II* |
DYS390 |
DYS391 |
DYS392 |
DYS393 |
1 |
14 |
13 |
17 |
23 |
10 |
11 |
12 |
2 |
13 |
13 |
18 |
24 |
10 |
11 |
13 |
3 |
14 |
13 |
16 |
23 |
10 |
13 |
13 |
4 |
14 |
12 |
16 |
24 |
11 |
13 |
13 |
5 |
14 |
13 |
17 |
24 |
10 |
13 |
13 |
6 |
14 |
13 |
16 |
25 |
11 |
13 |
13 |
7 |
14 |
13 |
16 |
23 |
11 |
13 |
13 |
8 |
14 |
13 |
16 |
24 |
11 |
13 |
13 |
9 |
14 |
13 |
17 |
24 |
11 |
13 |
13 |
10 |
14 |
13 |
16 |
24 |
11 |
14 |
13 |
11 |
14 |
14 |
16 |
24 |
11 |
13 |
13 |
12 |
14 |
14 |
16 |
23 |
11 |
13 |
13 |
13 |
15 |
12 |
17 |
22 |
10 |
11 |
14 |
14 |
15 |
13 |
16 |
23 |
11 |
13 |
13 |
15 |
15 |
13 |
16 |
24 |
11 |
13 |
13 |
16 |
15 |
14 |
17 |
25 |
11 |
11 |
13 |
17 |
13 |
13 |
17 |
24 |
10 |
11 |
13 |
18 |
14 |
12 |
16 |
23 |
10 |
11 |
13 |
19 |
14 |
13 |
16 |
23 |
10 |
11 |
12 |
20 |
14 |
13 |
16 |
24 |
10 |
13 |
13 |
21 |
14 |
13 |
16 |
25 |
10 |
13 |
13 |
22 |
16 |
13 |
18 |
24 |
11 |
11 |
13 |
23 |
15 |
13 |
16 |
23 |
9 |
11 |
12 |
24 |
15 |
13 |
16 |
24 |
11 |
11 |
13 |
25 |
16 |
13 |
17 |
25 |
10 |
11 |
13 |
26 |
14 |
12 |
16 |
22 |
10 |
11 |
13 |
27 |
14 |
13 |
16 |
24 |
10 |
14 |
13 |
28 |
14 |
13 |
16 |
25 |
11 |
14 |
13 |
29 |
13 |
13 |
17 |
24 |
10 |
15 |
13 |
30 |
14 |
13 |
17 |
23 |
11 |
13 |
13 |
31 |
15 |
13 |
17 |
23 |
10 |
12 |
14 |
32 |
15 |
14 |
16 |
23 |
10 |
11 |
13 |
33 |
15 |
13 |
18 |
25 |
10 |
11 |
13 |
34 |
16 |
13 |
17 |
21 |
10 |
11 |
14 |
35 |
15 |
14 |
18 |
23 |
10 |
12 |
15 |
36 |
16 |
13 |
16 |
23 |
11 |
12 |
14 |
37 |
17 |
13 |
17 |
25 |
10 |
11 |
13 |
38 |
14 |
13 |
15 |
23 |
11 |
13 |
13 |
39 |
14 |
14 |
16 |
24 |
10 |
13 |
13 |
40 |
15 |
12 |
17 |
22 |
10 |
11 |
13 |
41 |
15 |
13 |
16 |
24 |
10 |
12 |
15 |
42 |
14 |
14 |
16 |
23 |
10 |
13 |
13 |
43 |
15 |
12 |
16 |
22 |
10 |
11 |
13 |
44 |
16 |
13 |
16 |
25 |
10 |
11 |
13 |
45 |
17 |
13 |
16 |
23 |
10 |
11 |
13 |
46 |
13 |
14 |
16 |
24 |
9 |
11 |
13 |
47 |
14 |
12 |
17 |
22 |
10 |
11 |
13 |
48 |
15 |
12 |
16 |
24 |
10 |
11 |
12 |
49 |
15 |
13 |
18 |
21 |
10 |
11 |
13 |
Discrete-Laplace frequency estimation (Y17)
- Release
- R69
- Loci included
- DYS19, DYS389I, DYS389II*, DYS390, DYS391, DYS392, DYS393, DYS437, DYS438, DYS439, DYS448, DYS456, DYS458, DYS635, YGATAH4
- Central haplotypes
- 46
- EM converged
- true
- EM iterations
- 44
- GLM method
- internal_coef
- Init method
- pam
- Threshold frequency
- 1 in 72,176,110
- Per locus details
- DL centers distribution (download PDF)
Table of haplotype centers (click to show/hide)
|
DYS19 |
DYS389I |
DYS389II* |
DYS390 |
DYS391 |
DYS392 |
DYS393 |
DYS437 |
DYS438 |
DYS439 |
DYS448 |
DYS456 |
DYS458 |
DYS635 |
YGATAH4 |
1 |
16 |
12 |
16 |
25 |
11 |
11 |
13 |
15 |
10 |
11 |
21 |
14 |
16 |
21 |
10 |
2 |
14 |
13 |
17 |
23 |
10 |
11 |
12 |
15 |
9 |
11 |
20 |
15 |
17 |
23 |
12 |
3 |
14 |
13 |
16 |
24 |
11 |
13 |
13 |
15 |
12 |
12 |
19 |
16 |
16 |
23 |
12 |
4 |
14 |
13 |
16 |
24 |
10 |
13 |
13 |
15 |
12 |
12 |
19 |
16 |
18 |
23 |
12 |
5 |
14 |
13 |
16 |
24 |
10 |
13 |
13 |
15 |
12 |
12 |
19 |
16 |
17 |
23 |
12 |
6 |
15 |
14 |
18 |
23 |
10 |
12 |
14 |
14 |
10 |
11 |
20 |
15 |
15 |
21 |
11 |
7 |
14 |
13 |
16 |
24 |
11 |
13 |
13 |
15 |
12 |
12 |
19 |
15 |
17 |
23 |
12 |
8 |
14 |
13 |
16 |
24 |
11 |
13 |
13 |
15 |
12 |
12 |
19 |
15 |
18 |
23 |
12 |
9 |
14 |
13 |
16 |
25 |
11 |
14 |
13 |
15 |
12 |
12 |
18 |
17 |
17 |
23 |
12 |
10 |
14 |
13 |
16 |
23 |
11 |
13 |
13 |
15 |
12 |
12 |
19 |
17 |
17 |
23 |
11 |
11 |
13 |
13 |
17 |
24 |
10 |
11 |
13 |
14 |
10 |
12 |
20 |
15 |
16 |
22 |
11 |
12 |
15 |
12 |
17 |
22 |
10 |
11 |
14 |
16 |
10 |
11 |
21 |
15 |
16 |
20 |
12 |
13 |
16 |
13 |
18 |
24 |
11 |
11 |
13 |
15 |
10 |
12 |
20 |
15 |
17 |
23 |
11 |
14 |
14 |
13 |
16 |
23 |
11 |
13 |
13 |
15 |
12 |
12 |
19 |
16 |
17 |
25 |
12 |
15 |
15 |
13 |
17 |
25 |
11 |
11 |
13 |
14 |
11 |
10 |
20 |
16 |
15 |
23 |
13 |
16 |
14 |
13 |
16 |
24 |
11 |
13 |
13 |
15 |
12 |
12 |
19 |
16 |
18 |
23 |
12 |
17 |
14 |
12 |
16 |
22 |
10 |
11 |
13 |
16 |
10 |
11 |
20 |
14 |
15 |
23 |
11 |
18 |
14 |
12 |
16 |
22 |
10 |
11 |
13 |
16 |
10 |
11 |
20 |
14 |
15 |
21 |
11 |
19 |
14 |
13 |
17 |
24 |
10 |
13 |
13 |
15 |
12 |
12 |
19 |
15 |
18 |
24 |
13 |
20 |
14 |
13 |
16 |
23 |
11 |
13 |
13 |
15 |
12 |
11 |
19 |
16 |
17 |
23 |
12 |
21 |
14 |
13 |
16 |
24 |
11 |
13 |
13 |
14 |
12 |
12 |
18 |
15 |
17 |
23 |
11 |
22 |
15 |
12 |
17 |
22 |
10 |
11 |
14 |
16 |
10 |
12 |
21 |
15 |
17 |
21 |
11 |
23 |
16 |
13 |
17 |
25 |
10 |
11 |
13 |
14 |
11 |
11 |
20 |
16 |
16 |
23 |
12 |
24 |
14 |
12 |
16 |
22 |
10 |
11 |
13 |
16 |
10 |
11 |
20 |
14 |
15 |
22 |
11 |
25 |
14 |
13 |
16 |
24 |
10 |
13 |
13 |
15 |
12 |
11 |
19 |
15 |
17 |
24 |
12 |
26 |
14 |
13 |
16 |
23 |
10 |
13 |
13 |
15 |
12 |
11 |
19 |
15 |
16 |
23 |
12 |
27 |
14 |
13 |
16 |
24 |
11 |
13 |
13 |
15 |
12 |
12 |
19 |
16 |
17 |
23 |
12 |
28 |
15 |
13 |
16 |
23 |
10 |
11 |
13 |
14 |
10 |
12 |
18 |
14 |
19 |
21 |
11 |
29 |
15 |
13 |
16 |
23 |
10 |
13 |
13 |
14 |
9 |
11 |
19 |
15 |
17 |
21 |
11 |
30 |
15 |
12 |
16 |
24 |
10 |
11 |
12 |
16 |
9 |
12 |
19 |
13 |
16 |
21 |
11 |
31 |
14 |
13 |
16 |
24 |
11 |
13 |
13 |
15 |
12 |
12 |
19 |
15 |
16 |
23 |
12 |
32 |
15 |
13 |
16 |
23 |
9 |
11 |
12 |
14 |
9 |
12 |
21 |
16 |
14 |
21 |
12 |
33 |
15 |
13 |
17 |
21 |
10 |
11 |
13 |
14 |
11 |
12 |
21 |
15 |
16 |
21 |
11 |
34 |
13 |
13 |
17 |
24 |
10 |
11 |
13 |
14 |
10 |
12 |
20 |
16 |
15 |
22 |
12 |
35 |
15 |
14 |
16 |
22 |
10 |
11 |
12 |
14 |
9 |
11 |
19 |
15 |
17 |
21 |
12 |
36 |
15 |
13 |
18 |
25 |
10 |
11 |
13 |
14 |
11 |
10 |
20 |
15 |
15 |
24 |
12 |
37 |
15 |
13 |
17 |
23 |
10 |
12 |
15 |
14 |
10 |
11 |
20 |
14 |
15 |
21 |
10 |
38 |
15 |
14 |
16 |
23 |
11 |
14 |
14 |
14 |
10 |
10 |
19 |
14 |
17 |
22 |
12 |
39 |
17 |
13 |
15 |
23 |
10 |
11 |
13 |
15 |
10 |
12 |
21 |
14 |
17 |
22 |
12 |
40 |
16 |
13 |
16 |
23 |
11 |
12 |
14 |
15 |
10 |
11 |
20 |
17 |
15 |
21 |
11 |
41 |
15 |
13 |
16 |
24 |
10 |
12 |
15 |
15 |
10 |
11 |
20 |
14 |
16 |
19 |
11 |
42 |
13 |
14 |
16 |
24 |
9 |
11 |
13 |
14 |
10 |
10 |
20 |
16 |
18 |
21 |
12 |
43 |
14 |
13 |
16 |
23 |
10 |
11 |
12 |
15 |
9 |
11 |
20 |
15 |
15 |
21 |
11 |
44 |
13 |
13 |
17 |
24 |
10 |
14 |
13 |
14 |
11 |
12 |
20 |
15 |
16 |
22 |
12 |
45 |
13 |
12 |
16 |
23 |
10 |
13 |
14 |
14 |
11 |
12 |
20 |
15 |
18 |
22 |
12 |
46 |
14 |
13 |
16 |
23 |
10 |
10 |
14 |
16 |
11 |
10 |
19 |
15 |
17 |
25 |
12 |
* Please note that DYS389I was substracted from DYS389II
Population studies
- Kayser M., Brauer S., Schädlich H., Prinz M., Batzer MA., Zimmerman PA., Boatin BA. and Stoneking M. (2003), 'Y chromosome STR haplotypes and the genetic structure of U.S. populations of African, European, and Hispanic ancestry.', Genome Res 13(4):624-34 [PubMed] [DOI]
- Ge J., Budowle B., Planz JV., Eisenberg AJ., Ballantyne J. and Chakraborty R. (2010), 'US forensic Y-chromosome short tandem repeats database.', Leg Med (Tokyo) 12(6):289-95 [PubMed] [DOI]
- Frank WE., Ellinger ER. and Krishack PA. (2006), 'Y chromosome STR haplotypes and allele frequencies in Illinois Caucasian, African American, and Hispanic males.', J Forensic Sci 51(5):1207-15 [PubMed] [DOI]
- Steffen CR., Huszar TI., Borsuk LA., Vallone PM. and Gettings KB. (2022), 'A multi-dimensional evaluation of the ‘NIST 1032’ sample set across four forensic Y-STR multiplexes', For Sci Int Genet 57:102655 [DOI]
- Budowle B., Ge J., Aranda XG., Planz JV., Eisenberg AJ. and Chakraborty R. (2009), 'Texas population substructure and its impact on estimating the rarity of Y STR haplotypes from DNA evidence*.', J Forensic Sci 54(5):1016-21 [PubMed] [DOI]
- Xu H., Wang CC., Shrestha R., Wang LX., Zhang M., He Y., Kidd JR., Kidd KK., Jin L. and Li H. (2015), 'Inferring population structure and demographic history using Y‐STR data from worldwide populations', Mol Genet Genomics 290(1):141-50 [DOI]
- Pignone ML., Manzella AM., Galusha M., Le J. and Moreno LI. (2022), 'Y-STR Sample Haplotypes From Five United States of America Population Groups', Forensic Science International: Reports 5:100274 [DOI]
- Valverde L., Rosique M., Köhnemann S., Cardoso S., García A., Odriozola A., Aznar JM., Celorrio D., Schuerenkamp M., Zubizarreta J., Davis MC., Hampikian G., Pfeiffer H. and Pancorbo D. (2012), 'Y-STR variation in the Basque diaspora in the Western USA: evolutionary and forensic perspectives.', Int J Legal Med 126(2):293-8 [PubMed] [DOI]
- Purps J., Siegert S., Willuweit S., Nagy M., Alves C., Salazar R., Angustia SM., Santos LH., Anslinger K., Bayer B., Ayub Q., Wei W., Xue Y., Tyler-Smith C., Bafalluy MB., Martínez-Jarreta B., Egyed B., Balitzki B., Tschumi S., Ballard D., Court DS., Barrantes X., Bäßler G., Wiest T., Berger B., Niederstätter H., Parson W., Davis C., Budowle B., Burri H., Borer U., Koller C., Carvalho EF., Domingues PM., Chamoun WT., Coble MD., Hill CR., Corach D., Caputo M., D'Amato ME., Davison S., Decorte R., Larmuseau MH., Ottoni C., Rickards O., Lu D., Jiang C., Dobosz T., Jonkisz A., Frank WE., Furac I., Gehrig C., Castella V., Grskovic B., Haas C., Wobst J., Hadzic G., Drobnic K., Honda K., Hou Y., Zhou D., Li Y., Hu S., Chen S., Immel UD., Lessig R., Jakovski Z., Ilievska T., Klann AE., García CC., Knijff D., Kraaijenbrink T., Kondili A., Miniati P., Vouropoulou M., Kovacevic L., Marjanovic D., Lindner I., Mansour I., Al-Azem M., Andari AE., Marino M., Furfuro S., Locarno L., Martín P., Luque GM., Alonso A., Miranda LS., Moreira H., Mizuno N., Iwashima Y., Neto RS., Nogueira TL., Silva R., Nastainczyk-Wulf M., Edelmann J., Kohl M., Nie S., Wang X., Cheng B., Núñez C., Pancorbo MM., Olofsson JK., Morling N., Onofri V., Tagliabracci A., Pamjav H., Volgyi A., Barany G., Pawlowski R., Maciejewska A., Pelotti S., Pepinski W., Abreu-Glowacka M., Phillips C., Cárdenas J., Rey-Gonzalez D., Salas A., Brisighelli F., Capelli C., Toscanini U., Piccinini A., Piglionica M., Baldassarra SL., Ploski R., Konarzewska M., Jastrzebska E., Robino C., Sajantila A., Palo JU., Guevara E., Salvador J., Ungria MC., Rodriguez JJ., Schmidt U., Schlauderer N., Saukko P., Schneider PM., Sirker M., Shin KJ., Oh YN., Skitsa I., Ampati A., Smith TG., Calvit LS., Stenzl V., Capal T., Tillmar A., Nilsson H., Turrina S., Leo D., Verzeletti A., Cortellini V., Wetton JH., Gwynne GM., Jobling MA., Whittle MR., Sumita DR., Wolańska-Nowak P., Yong RY., Krawczak M., Nothnagel M. and Roewer L. (2014), 'A global analysis of Y-chromosomal haplotype diversity for 23 STR loci.', Forensic Sci Int Genet 12:12-23 [PubMed] [DOI]