A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608475



Internal ID21800522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98273274..98284828hg38UCSC Ensembl
chr15:98816503..98828057hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3811555
hg1911555
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023543
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608475
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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