A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585545



Internal ID16026268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14897008..14930357hg38UCSC Ensembl
Innerchr20:14877654..14911003hg19UCSC Ensembl
Innerchr20:14825654..14859003hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3833350
hg1933350
hg1833350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7484n54
Supporting Variantsnssv938174
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)nsv585545
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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