A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875708



Internal ID15822978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60335374..60336897hg38UCSC Ensembl
Innerchr17:58412735..58414258hg19UCSC Ensembl
Innerchr17:55767517..55769040hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381524
hg191524
hg181524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575822
Supporting Variants
Samples
Known GenesUSP32
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv875708
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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