A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585153



Internal ID346732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80088489..80089216hg38UCSC Ensembl
Outerchr11:80086506..80090119hg38UCSC Ensembl
Innerchr11:79799533..79800260hg19UCSC Ensembl
Outerchr11:79797550..79801163hg19UCSC Ensembl
Innerchr11:79477181..79477908hg18UCSC Ensembl
Outerchr11:79475198..79478811hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg383614
hg193614
hg183614
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv274950
Supporting Variants
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)essv2585153
Frequency
Sample Size1250
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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