A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938719



Internal ID26543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120257420..120257485hg38UCSC Ensembl
chr3:119976267..119976332hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139419
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938719
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002499


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