A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934402



Internal ID23666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:83223742..83865464hg38UCSC Ensembl
chr3:83272893..83914615hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38641723
hg19641723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447987
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934402
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer