A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585262



Internal ID16025985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:2182010..2309687hg38UCSC Ensembl
Innerchr20:2162656..2290333hg19UCSC Ensembl
Innerchr20:2110656..2238333hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38127678
hg19127678
hg18127678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937303
Samples
Known GenesTGM3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585262
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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