A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615549



Internal ID21807596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45497806..45497806hg38UCSC Ensembl
chr13:46071941..46071941hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6099278
Supporting Variants
Samples
Known GenesCOG3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615549
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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