A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611703



Internal ID21803750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49762104..49762156hg38UCSC Ensembl
chr13:50336240..50336292hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039769
Supporting Variants
Samples
Known GenesKPNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611703
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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