A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797511



Internal ID18833221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94211379..94296722hg38UCSC Ensembl
Innerchr11:93944545..94029888hg19UCSC Ensembl
Innerchr11:93584193..93669536hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3885344
hg1985344
hg1885344
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892069
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797511
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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