A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892040



Internal ID19186436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:83847695..83875794hg38UCSC Ensembl
Outerchr11:83847695..83881354hg38UCSC Ensembl
Innerchr11:83558738..83586837hg19UCSC Ensembl
Outerchr11:83558738..83592397hg19UCSC Ensembl
Innerchr11:83236386..83264485hg18UCSC Ensembl
Outerchr11:83236386..83270045hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3833660
hg1933660
hg1833660
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789921, essv25789248, essv25787809, essv25789952, essv25790981, essv25790701, essv25792332, essv25791372, essv25788523
Samples
Known GenesDLG2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892040
Frequency
Sample Size3017
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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