The IndiGenomes resource encompasses the genomic data from over 1000 whole genome
sequences sequenced from across India as part of the IndiGen programme and represents diverse
geographies and ethnicities. The resource provides access to over 55 million genetic variants
comprising of single nucleotide variants and indels. The variants are systematically annotated
according to the recent Genome Reference Consortium Human Build 38 (GRCh38). Clinically
relevant annotations as well as allele frequencies from global populations have also been integrated.