A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616176



Internal ID21808223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65449585..65449585hg38UCSC Ensembl
chr15:65741923..65741923hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6083798
Supporting Variants
Samples
Known GenesDPP8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616176
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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