A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892052



Internal ID19186448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:88013627..88072131hg38UCSC Ensembl
Outerchr11:88013627..88088650hg38UCSC Ensembl
Innerchr11:87746795..87805299hg19UCSC Ensembl
Outerchr11:87746795..87821818hg19UCSC Ensembl
Innerchr11:87386443..87444947hg18UCSC Ensembl
Outerchr11:87386443..87461466hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3875024
hg1975024
hg1875024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801016, essv25784606, essv25785306, essv25800079, essv25800438, essv25780186
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892052
Frequency
Sample Size3017
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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