A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875664



Internal ID15822934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60335053..60336225hg38UCSC Ensembl
Innerchr17:58412414..58413586hg19UCSC Ensembl
Innerchr17:55767196..55768368hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381173
hg191173
hg181173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575812
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)nssv875664
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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