A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598924



Internal ID21790969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65802040..65802040hg38UCSC Ensembl
chr15:66094378..66094378hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6096952
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598924
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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