A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932350



Internal ID22290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32578796..32578935hg38UCSC Ensembl
chr3:32620288..32620427hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438288
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932350
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001406


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