A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585533



Internal ID16026256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14820707..14940960hg38UCSC Ensembl
Innerchr20:14801353..14921606hg19UCSC Ensembl
Innerchr20:14749353..14869606hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38120254
hg19120254
hg18120254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938166
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)nsv585533
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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