Submission GVM001119
2025-07-23
BGI-Shenzhen
OrganismHomo sapiens
Version GRCh38
BioProjectPRJCA043552
Sample numbers6685
Abstract

The whole-genome sequencing variants data (vcf) includes SNPs and indels variants information limited to the 84 genes recommended by the ACMG SF v3.3 in 6685 newborns in Qingdao, China.

Data Accessibility:Controlled access   
Release date2025-07-22
Available data
data submitter: gaoya@genomics.cn
QDnewborn6685s.annovar.SF3.3.gene.all.vcf.gz
QDnewborn6685s.annovar.SF3.3.gene.all.vcf.gz.tbi