A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929938



Internal ID20698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3957458..4160267hg38UCSC Ensembl
chr3:3999142..4201951hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38202810
hg19202810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435439
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929938
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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