A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938725



Internal ID26546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120357023..120357082hg38UCSC Ensembl
chr3:120075870..120075929hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437659
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938725
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001093


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