A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517913



Internal ID21842272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46275838..46275838hg38UCSC Ensembl
chr1:46741510..46741510hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052388
Supporting Variants
Samples
Known GenesRAD54L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17517913
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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