Information on the National Database "Indonesia"

The National Database "Indonesia" consists of 278 haplotypes (at least minimal) which were published in 2 population studies and were additionally submitted via personal communication (1 submission) .

Most common haplotypes

Count DYS19 DYS389I DYS389II DYS390 DYS391 DYS392 DYS393 DYS385
14 15 12 28 24 11 13 13 11,16
6 17 12 29 21 9 12 13 12,15
5 16 12 28 23 10 12 14 12,14
4 14 13 29 23 10 10 14 13,19
4 15 12 27 23 10 14 13 13,13
4 15 12 28 21 10 11 12 11,16
4 15 12 28 23 10 14 13 13,14
3 15 12 28 21 11 11 12 11,17
3 15 12 28 23 10 12 14 12,14
3 15 12 28 24 10 13 13 12,17
Count DYS391 DYS389I DYS439 DYS389II DYS438 DYS437 DYS19 DYS392 DYS393 DYS390 DYS385
9 11 12 12 28 10 15 15 13 13 24 11,16
6 9 12 11 29 10 14 17 12 13 21 12,15
4 10 13 10 29 11 16 14 10 14 23 13,19
4 11 12 13 28 10 15 15 13 13 24 11,16
3 10 12 11 28 10 14 16 12 14 23 12,14
3 11 12 11 28 10 14 15 11 12 21 11,17
3 11 13 12 29 10 14 15 13 14 25 18,20
2 10 12 11 28 10 14 15 11 12 21 11,16
2 10 12 11 28 10 14 15 11 12 21 11,17
2 10 12 11 28 10 14 15 14 13 23 13,14
Count DYS456 DYS389I DYS390 DYS389II DYS458 DYS19 DYS385 DYS393 DYS391 DYS439 DYS635 DYS392 YGATAH4 DYS437 DYS438 DYS448
7 15 12 24 28 15 15 11,16 13 11 12 21 13 12 15 10 19
4 15 12 24 28 15 15 11,16 13 11 13 21 13 12 15 10 19
4 15 13 23 29 17 14 13,19 14 10 10 26 10 12 16 11 19
3 15 12 21 29 14 17 12,15 13 9 11 22 12 13 14 10 17
3 16 13 25 29 16 15 18,20 14 11 12 23 13 10 14 10 19
2 15 12 21 28 17 15 11,16 12 10 13 23 11 11 16 10 20
2 15 12 21 28 17 15 11,17 12 10 11 24 11 10 14 10 21
2 15 12 21 28 17 15 11,17 12 11 11 24 11 10 14 10 21
2 15 12 23 28 18 15 13,14 13 10 11 21 14 11 14 10 17
2 15 12 24 29 16 15 11,16 13 10 12 21 13 12 15 10 19

 There are no Y23 haplotypes or all haplotypes are singletons.

 There are no Y27 haplotypes or all haplotypes are singletons.

 There are no Ymax haplotypes or all haplotypes are singletons.

Population studies

  • Kim YJ., Shin DJ., Kim JM., Jin HJ., Kwak KD., Han MS., Choi SK. and Kim W. (2001), 'Y-chromosome STR haplotype profiling in the Korean population.', Forensic Sci Int 115(3):231-7 [PubMed]
  • Ballantyne KN., Ralf A., Aboukhalid R., Niaz M., Anjos MJ., Ayub Q., Balažic J., Ballantyne J., David J., Berger B., Bobillo C., Bouabdellah M., Burri H., Capal T., Caratti S., Cárdenas J., Cartault F., Elizeu F., Carvalho M., Cheng B., Michael D., Comas D., Corach D., Maria E., Davison S., De P., Corazon M., Decorte R., Dobosz T., Berit M., Elmrghni S., Gliwiński M., Sara C., Grol L., Haas C., Hanson E., Henke J., Henke L., Herrera-Rodríguez F., Carolyn R., Holmlund G., Honda K., Immel UD., Inokuchi S., Mark A., Kaddura M., Jong S., Soon H., Kim W., Turi E., Klausriegler E., Kling D., Kovačević L., Kovatsi L., Krajewski P., Kravchenko S., Maarten H., Young E., Lessig R., Ludmila A., Marjanović D., Minarik M., Mizuno N., Moreira H., Morling N., Mukherjee M., Munier P., Nagaraju J., Neuhuber F., Nie S., Nilasitsataporn P., Nishi T., Hye H., Olofsson J., Onofri V., Jukka U., Pamjav H., Parson W., Petlach M., Phillips C., Ploski R., Samayamantri P., Primorac D., Gludhug A., Purps J., Rangel-Villalobos H., Rębała K., Rerkamnuaychoke B., Rey D., Robino C., Roewer L., Rosa A., Sajantila A., Sala A., Jazelyn M., Sanz P., Schmitt C., Anil K., Dayse A., Shin KJ., Sijen T., Sirker M., Siváková D., Škaro V., Solano-Matamoros C., Souto L., Stenzl V., Sudoyo H., Syndercombe-Court D., Tagliabracci A., Taylor D., Tillmar A., Iosif S., Tyler-Smith C., Kristiaan J., Vanek D., Völgyi A., Ward D., Willemse P., Eric PH., Rita YY., Zupanič I., KayserAmato M., Davison S., De P., Corazon M., Decorte R., Dobosz T., Berit M., Elmrghni S., Gliwiński M., Sara C., Grol L., Haas C., Hanson E., Henke J., Henke L., Herrera-Rodríguez F., Carolyn R., Holmlund G., Honda K., Immel UD., Inokuchi S., Mark A., Kaddura M., Jong S., Soon H., Kim W., Turi E., Klausriegler E., Kling D., Kovačević L., Kovatsi L., Krajewski P., Kravchenko S., Maarten H., Young E., Lessig R., Ludmila A., Marjanović D., Minarik M., Mizuno N., Moreira H., Morling N., Mukherjee M., Munier P., Nagaraju J., Neuhuber F., Nie S., Nilasitsataporn P., Nishi T., Hye H., Olofsson J., Onofri V., Jukka U., Pamjav H., Parson W., Petlach M., Phillips C., Ploski R., Samayamantri P., Primorac D., Gludhug A., Purps J., Rangel-Villalobos H., Rębała K., Rerkamnuaychoke B., Rey D., Robino C., Roewer L., Rosa A., Sajantila A., Sala A., Jazelyn M., Sanz P., Schmitt C., Anil K., Dayse A., Shin KJ., Sijen T., Sirker M., Siváková D., Škaro V., Solano-Matamoros C., Souto L., Stenzl V., Sudoyo H., Syndercombe-Court D., Tagliabracci A., Taylor D., Tillmar A., Iosif S., Tyler-Smith C., Kristiaan J., Vanek D., Völgyi A., Ward D., Willemse P., Eric PH., Rita YY., Zupanič I. and Kayser M. (2014), 'Toward Male Individualization with Rapidly Mutating Y-Chromosomal Short Tandem Repeats', Human Mutation 35(8):1021-1032 [DOI]

Personal communication

YA002928
* See FAQ/Glossary (http://yhrd.org/pages/faq) for further explanations of abbreviated terms used here