A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575807



Internal ID16016530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60335000..60336165hg38UCSC Ensembl
Innerchr17:58412361..58413526hg19UCSC Ensembl
Innerchr17:55767143..55768308hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381166
hg191166
hg181166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5734n54
Supporting Variantsnssv875651, nssv875652
Samples
Known GenesUSP32
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575807
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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