A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611290



Internal ID21803337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70531385..70531385hg38UCSC Ensembl
chr15:70823724..70823724hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6093129
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611290
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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