A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798627



Internal ID19171268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:82256158..82320392hg38UCSC Ensembl
Innerchr11:81967200..82031434hg19UCSC Ensembl
Innerchr11:81644848..81709082hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3864235
hg1964235
hg1864235
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892038
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798627
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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