A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931560



Internal ID21784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39427684..39427737hg38UCSC Ensembl
chr3:39469175..39469228hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140024
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931560
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.016399


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