A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586732



Internal ID16374141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64059960..64159119hg38UCSC Ensembl
Innerchr20:62691313..62790472hg19UCSC Ensembl
Innerchr20:62161757..62260916hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3899160
hg1999160
hg1899160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv944157
Samples
Known GenesC20orf201, MIR6813, NPBWR2, OPRL1, RGS19, TCEA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586732
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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