A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792593



Internal ID19175559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80657312..81113098hg38UCSC Ensembl
Innerchr11:80368356..80824141hg19UCSC Ensembl
Innerchr11:80046004..80501789hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38455787
hg19455786
hg18455786
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892031
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=100
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792593
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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