A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892031



Internal ID19186427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80657312..81113098hg38UCSC Ensembl
Outerchr11:80657312..81113098hg38UCSC Ensembl
Innerchr11:80368356..80824141hg19UCSC Ensembl
Outerchr11:80368356..80824141hg19UCSC Ensembl
Innerchr11:80046004..80501789hg18UCSC Ensembl
Outerchr11:80046004..80501789hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38455787
hg19455786
hg18455786
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792593
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892031
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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