A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585464



Internal ID16026187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14725242..15101900hg38UCSC Ensembl
Innerchr20:14705888..15082546hg19UCSC Ensembl
Innerchr20:14653888..15030546hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38376659
hg19376659
hg18376659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7469n54
Supporting Variantsnssv938062
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)nsv585464
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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