A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892068



Internal ID18839778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93819689..93897325hg38UCSC Ensembl
Outerchr11:93819689..93897325hg38UCSC Ensembl
Innerchr11:93552855..93630491hg19UCSC Ensembl
Outerchr11:93552855..93630491hg19UCSC Ensembl
Innerchr11:93192503..93270139hg18UCSC Ensembl
Outerchr11:93192503..93270139hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3877637
hg1977637
hg1877637
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788122
Samples
Known GenesVSTM5
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892068
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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