A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585437



Internal ID16372846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:13914223..13958143hg38UCSC Ensembl
Innerchr20:13894869..13938789hg19UCSC Ensembl
Innerchr20:13842869..13886789hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3843921
hg1943921
hg1843921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938037
Samples
Known GenesSEL1L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585437
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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