A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932231



Internal ID22211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37319222..37878022hg38UCSC Ensembl
chr3:37360713..37919513hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38558801
hg19558801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441925
Supporting Variants
Samples
Known GenesC3orf35, CTDSPL, GOLGA4, ITGA9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932231
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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