A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938179



Internal ID16232135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14903655..15014697hg38UCSC Ensembl
Innerchr20:14884301..14995343hg19UCSC Ensembl
Innerchr20:14832301..14943343hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38111043
hg19111043
hg18111043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585551
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)nssv938179
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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