A curated catalogue of human genomic structural variation




Variant Details

Variant: esv274869



Internal ID347829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124906079..124907510hg38UCSC Ensembl
Outerchr11:124901623..124918760hg38UCSC Ensembl
Innerchr11:124775975..124777406hg19UCSC Ensembl
Outerchr11:124771519..124788656hg19UCSC Ensembl
Innerchr11:124281185..124282616hg18UCSC Ensembl
Outerchr11:124276729..124293866hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3817138
hg1917138
hg1817138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585271
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)esv274869
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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