A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627678



Internal ID7014506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108468960..108470813hg38UCSC Ensembl
Innerchr11:108468985..108470789hg38UCSC Ensembl
Outerchr11:108468936..108470838hg38UCSC Ensembl
chr11:108339687..108341540hg19UCSC Ensembl
Innerchr11:108339712..108341516hg19UCSC Ensembl
Outerchr11:108339663..108341565hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381854
hg191854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14278411, essv14278415, essv14278412, essv14278410, essv14278413, essv14278414
SamplesNA19377, NA19379, NA19461, NA19017, NA19401, NA19473
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627678
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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