A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938079



Internal ID15885349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14781064..14903655hg38UCSC Ensembl
Innerchr20:14761710..14884301hg19UCSC Ensembl
Innerchr20:14709710..14832301hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38122592
hg19122592
hg18122592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585487
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)nssv938079
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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