A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604634



Internal ID21796681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55325498..55325498hg38UCSC Ensembl
chr15:55617696..55617696hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6099582
Supporting Variants
Samples
Known GenesPIGB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604634
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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