A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7467n54



Internal ID22775362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14701217..14909565hg38UCSC Ensembl
chr20:14681863..14890211hg19UCSC Ensembl
chr20:14629863..14838211hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38208349
hg19208349
hg18208349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585466, nsv585463, nsv585462, nsv585458
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)dgv7467n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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