A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599938



Internal ID21791985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26972737..26972737hg38UCSC Ensembl
chr13:27546874..27546874hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087166
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599938
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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