A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575819



Internal ID16016542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60335320..60361657hg38UCSC Ensembl
Innerchr17:58412681..58439018hg19UCSC Ensembl
Innerchr17:55767463..55793800hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3826338
hg1926338
hg1826338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5736n54
Supporting Variantsnssv875689
Samples
Known GenesUSP32
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575819
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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