A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606078



Internal ID21798125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34107952..34138754hg38UCSC Ensembl
chr15:34400153..34430955hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3830803
hg1930803
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032809
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606078
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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