A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585477



Internal ID16026200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14759193..14886776hg38UCSC Ensembl
Innerchr20:14739839..14867422hg19UCSC Ensembl
Innerchr20:14687839..14815422hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38127584
hg19127584
hg18127584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7473n54
Supporting Variantsnssv938073
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585477
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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