A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585466



Internal ID16026189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14725970..14882326hg38UCSC Ensembl
Innerchr20:14706616..14862972hg19UCSC Ensembl
Innerchr20:14654616..14810972hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38156357
hg19156357
hg18156357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7467n54
Supporting Variantsnssv938064
Samples
Known GenesMACROD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585466
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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