A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797013



Internal ID19178986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80434987..80469482hg38UCSC Ensembl
Innerchr11:80146031..80180526hg19UCSC Ensembl
Innerchr11:79823679..79858174hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3834496
hg1934496
hg1834496
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892030
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797013
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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