A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586082



Internal ID16373491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45575651..45576975hg38UCSC Ensembl
Innerchr20:44204290..44205614hg19UCSC Ensembl
Innerchr20:43637704..43639028hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg381325
hg191325
hg181325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7587n54
Supporting Variantsnssv940718, nssv940719, nssv940717
Samples
Known GenesWFDC8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586082
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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