A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598279



Internal ID21790323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:59667764..59667764hg38UCSC Ensembl
chr13:60241898..60241898hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097539
Supporting Variants
Samples
Known GenesDIAPH3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598279
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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