A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892029



Internal ID19186425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:79113278..79180160hg38UCSC Ensembl
Outerchr11:79113278..79180160hg38UCSC Ensembl
Innerchr11:78824323..78891205hg19UCSC Ensembl
Outerchr11:78824323..78891205hg19UCSC Ensembl
Innerchr11:78501971..78568853hg18UCSC Ensembl
Outerchr11:78501971..78568853hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3866883
hg1966883
hg1866883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786775, essv25787544
Samples
Known GenesTENM4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892029
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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