A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586731



Internal ID16374140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64059960..64131533hg38UCSC Ensembl
Innerchr20:62691313..62762886hg19UCSC Ensembl
Innerchr20:62161757..62233330hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3871574
hg1971574
hg1871574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7701n54
Supporting Variantsnssv944156
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)nsv586731
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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