A curated catalogue of human genomic structural variation




Variant Details

Variant: esv274882



Internal ID347842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:59467591..59468133hg38UCSC Ensembl
Outerchr11:59463608..59469297hg38UCSC Ensembl
Innerchr11:59235064..59235606hg19UCSC Ensembl
Outerchr11:59231081..59236770hg19UCSC Ensembl
Innerchr11:58991640..58992182hg18UCSC Ensembl
Outerchr11:58987657..58993346hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg385690
hg195690
hg185690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585198
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)esv274882
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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