A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575820



Internal ID16016543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60335374..60336165hg38UCSC Ensembl
Innerchr17:58412735..58413526hg19UCSC Ensembl
Innerchr17:55767517..55768308hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38792
hg19792
hg18792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5737n54
Supporting Variantsnssv875693, nssv875690, nssv875691, nssv875692
Samples
Known GenesUSP32
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575820
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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