A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892087



Internal ID19186483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98553052..98585755hg38UCSC Ensembl
Outerchr11:98553052..98585755hg38UCSC Ensembl
Innerchr11:98423782..98456485hg19UCSC Ensembl
Outerchr11:98423782..98456485hg19UCSC Ensembl
Innerchr11:97928992..97961695hg18UCSC Ensembl
Outerchr11:97928992..97961695hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3832704
hg1932704
hg1832704
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790804
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892087
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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