A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603725



Internal ID21795772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65411500..65411500hg38UCSC Ensembl
chr15:65703838..65703838hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6090325
Supporting Variants
Samples
Known GenesIGDCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603725
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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