A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545453



Internal ID21869808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122747715..122747715hg38UCSC Ensembl
chr3:122466562..122466562hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061702
Supporting Variants
Samples
Known GenesHSPBAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545453
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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