A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627125



Internal ID7013955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87335664..87369438hg38UCSC Ensembl
Innerchr11:87335814..87369288hg38UCSC Ensembl
Outerchr11:87335514..87369588hg38UCSC Ensembl
chr11:87046706..87080480hg19UCSC Ensembl
Innerchr11:87046856..87080330hg19UCSC Ensembl
Outerchr11:87046556..87080630hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3833775
hg1933775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv215e214
Supporting Variantsessv14223718, essv14223719
SamplesHG03086, HG02085
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627125
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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