A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585664



Internal ID16026387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:18005414..18038630hg38UCSC Ensembl
Innerchr20:17986058..18019274hg19UCSC Ensembl
Innerchr20:17934058..17967274hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3833217
hg1933217
hg1833217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152368
SamplesHGDP00072
Known GenesOVOL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585664
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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