A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616901



Internal ID21808948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25898786..25898786hg38UCSC Ensembl
chr15:26143933..26143933hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094943
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616901
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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