A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892042



Internal ID19186438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84348565..84879474hg38UCSC Ensembl
Outerchr11:84348565..84879474hg38UCSC Ensembl
Innerchr11:84059608..84590518hg19UCSC Ensembl
Outerchr11:84059608..84590518hg19UCSC Ensembl
Innerchr11:83737256..84268166hg18UCSC Ensembl
Outerchr11:83737256..84268166hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38530910
hg19530911
hg18530911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782059
Samples
Known GenesDLG2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892042
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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