A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555490



Internal ID21879845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184235714..184235714hg38UCSC Ensembl
chr3:183953502..183953502hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6062219
Supporting Variants
Samples
Known GenesVWA5B2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17555490
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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