A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616854



Internal ID21808901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24198275..24297147hg38UCSC Ensembl
chr15:24443422..24542294hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3898873
hg1998873
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028508
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616854
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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