A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792866



Internal ID19173258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116506908..116541896hg38UCSC Ensembl
Innerchr11:116377625..116412613hg19UCSC Ensembl
Innerchr11:115882835..115917823hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3834989
hg1934989
hg1834989
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892102
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792866
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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