A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575806



Internal ID16016529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60335000..60335743hg38UCSC Ensembl
Innerchr17:58412361..58413104hg19UCSC Ensembl
Innerchr17:55767143..55767886hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38744
hg19744
hg18744
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875650
Samples
Known GenesUSP32
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575806
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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