A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517846



Internal ID21842205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32236915..32236915hg38UCSC Ensembl
chr2:32461984..32461984hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6049514
Supporting Variants
Samples
Known GenesNLRC4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17517846
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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