A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892085



Internal ID19186481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98113646..98294667hg38UCSC Ensembl
Outerchr11:98107926..98294667hg38UCSC Ensembl
Innerchr11:97984374..98165395hg19UCSC Ensembl
Outerchr11:97978654..98165395hg19UCSC Ensembl
Innerchr11:97489584..97670605hg18UCSC Ensembl
Outerchr11:97483864..97670605hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38186742
hg19186742
hg18186742
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790651, essv25789241
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892085
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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