A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938076



Internal ID15885346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14766825..14990808hg38UCSC Ensembl
Innerchr20:14747471..14971454hg19UCSC Ensembl
Innerchr20:14695471..14919454hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38223984
hg19223984
hg18223984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585480
Supporting Variants
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)nssv938076
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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