A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608081



Internal ID21800128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61317988..61317988hg38UCSC Ensembl
chr15:61610187..61610187hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095386
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608081
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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