A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929032



Internal ID20065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5031297..5032055hg38UCSC Ensembl
chr3:5072982..5073740hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38759
hg19759
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433998
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929032
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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