A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875661



Internal ID15822931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60335000..60345611hg38UCSC Ensembl
Innerchr17:58412361..58422972hg19UCSC Ensembl
Innerchr17:55767143..55777754hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3810612
hg1910612
hg1810612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575810
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)nssv875661
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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