A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585540



Internal ID16372949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14878264..15261719hg38UCSC Ensembl
Innerchr20:14858910..15242365hg19UCSC Ensembl
Innerchr20:14806910..15190365hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38383456
hg19383456
hg18383456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938170
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)nsv585540
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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