A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585462



Internal ID16026185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14725242..14878264hg38UCSC Ensembl
Innerchr20:14705888..14858910hg19UCSC Ensembl
Innerchr20:14653888..14806910hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38153023
hg19153023
hg18153023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7467n54
Supporting Variantsnssv938060
Samples
Known GenesMACROD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585462
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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