A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892038



Internal ID19186434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:82256158..82320392hg38UCSC Ensembl
Outerchr11:82256158..82320392hg38UCSC Ensembl
Innerchr11:81967200..82031434hg19UCSC Ensembl
Outerchr11:81967200..82031434hg19UCSC Ensembl
Innerchr11:81644848..81709082hg18UCSC Ensembl
Outerchr11:81644848..81709082hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3864235
hg1964235
hg1864235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798627, essv25782442, essv25783429
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892038
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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