A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096168



Internal ID21270330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:63499805..63508213hg38UCSC Ensembl
Innerchr15:63792004..63800412hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg388409
hg198409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115168
Supporting Variants
Samplessample149
Known GenesUSP3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096168
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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