A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892023



Internal ID18839733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67768190..67947557hg38UCSC Ensembl
Outerchr11:67734155..67964485hg38UCSC Ensembl
Innerchr11:67535661..67715028hg19UCSC Ensembl
Outerchr11:67501626..67731956hg19UCSC Ensembl
Innerchr11:67292237..67471604hg18UCSC Ensembl
Outerchr11:67258202..67488532hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38230331
hg19230331
hg18230331
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796569, essv25797058, essv25796038, essv25792301, essv25796091
Samples
Known GenesFAM86C2P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892023
Frequency
Sample Size3017
Observed Gain1
Observed Loss4
Observed Complex0
Frequencyn/a


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