A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585630



Internal ID16373039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:15354928..15380171hg38UCSC Ensembl
Innerchr20:15335574..15360816hg19UCSC Ensembl
Innerchr20:15283574..15308816hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3825244
hg1925243
hg1825243
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938517
Samples
Known GenesMACROD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585630
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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