A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585435



Internal ID16372844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:13429991..13601829hg38UCSC Ensembl
Innerchr20:13410638..13582476hg19UCSC Ensembl
Innerchr20:13358638..13530476hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38171839
hg19171839
hg18171839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7462n54
Supporting Variantsnssv938035
Samples
Known GenesTASP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585435
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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