A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938039



Internal ID16231995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14371748..14477188hg38UCSC Ensembl
Innerchr20:14352394..14457834hg19UCSC Ensembl
Innerchr20:14300394..14405834hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38105441
hg19105441
hg18105441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585440
Supporting Variants
Samples
Known GenesMACROD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv938039
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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