A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939631



Internal ID27141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136201696..136216116hg38UCSC Ensembl
chr3:135920538..135934958hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3814421
hg1914421
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448409
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939631
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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