A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585529



Internal ID16026252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14817871..15011896hg38UCSC Ensembl
Innerchr20:14798517..14992542hg19UCSC Ensembl
Innerchr20:14746517..14940542hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38194026
hg19194026
hg18194026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7479n54
Supporting Variantsnssv938163
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)nsv585529
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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