The 1000 Genomes Project is an international collaboration which has established the most detailed catalogue of human genetic variation, including SNPs, structural variants, and their haplotype contex
Distribution of CHs has been examined among all human autosomes in 5398 segments, and these data are shown in the Additional file 2: Table ST1. (XLSX 643 kb)
Table S1. List of the high coverage samples analysed in this study along with their geographic origin and Y-chromosome haplogroup affiliation. (XLSX 20 kb)
A small genotype data repository containing data used in recent papers from the Estonian Biocentre. Most of the data pertains to human population genetics. PDF files of the papers are also freely avai