A curated catalogue of human genomic structural variation




Variant Details

Variant: esv274868



Internal ID347828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:123276027..123281077hg38UCSC Ensembl
Outerchr11:123273375..123282040hg38UCSC Ensembl
Innerchr11:123146735..123151785hg19UCSC Ensembl
Outerchr11:123144083..123152748hg19UCSC Ensembl
Innerchr11:122651945..122656995hg18UCSC Ensembl
Outerchr11:122649293..122657958hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg388666
hg198666
hg188666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585181
Samples
Known Genes
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv274868
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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