A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892057



Internal ID18839767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89464315..89741019hg38UCSC Ensembl
Outerchr11:89464315..89741019hg38UCSC Ensembl
Innerchr11:89197483..89474187hg19UCSC Ensembl
Outerchr11:89197483..89474187hg19UCSC Ensembl
Innerchr11:88837131..89113835hg18UCSC Ensembl
Outerchr11:88837131..89113835hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38276705
hg19276705
hg18276705
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788721
Samples
Known GenesFOLH1B, NOX4, TRIM77
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892057
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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