The Y Chromosome Haplotype Reference Database (YHRD) is an open access, annotated collection of population samples typed for Y chromosomal sequence variants. Two important objectives are pursued: (1) the generation of reliable frequency estimates for Y-STR Haplotypes and Y-SNP Haplotypes to be used in the quantitative assessment of matches in forensic and kinship cases and (2) the characterization of male lineages to draw conclusions about the origins and history of human populations. Since its creation in 1999 it has been curated by Lutz Roewer and Sascha Willuweit at the Institute of Legal Medicine and Forensic Sciences, Charité - Universitätsmedizin Berlin. The database is endorsed by the International Society for Forensic Genetics (ISFG) and partially funded by Life Technologies and Promega Corporation. By June 2017 more than 188,000 9-locus haplotypes, among them 136,443 17-locus haplotypes, 34,133 23-locus haplotypes, 18,921 27-locus haplotypes and 20,495 Y SNP profiles from 1099 sampling locations in 132 countries have been directly submitted by more than 300 institutes and laboratories. In geographic terms, about 41% of the YHRD samples stem from Asia, 34% from Europe, 14% from Latin America, 5% from North America, 4% from Africa and 1% from Oceania/Australia. The individual sampling projects are described in 446 peer-reviewed publications
YHRD is built by direct submissions of population data from individual laboratories. Upon receipt of a submission, the YHRD staff examines the originality of the data and assigns an accession number to the population sample and performs quality assurance checks. The submissions are then released to the public database, where the entries are retrievable by Search for haplotypes, populations, contributors or accession numbers. All population data published in forensic journals as FSI: Genetics or International Journal of Legal Medicine are required to be validated by the YHRD custodians and are subsequently included in the YHRD.