A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627346



Internal ID7014176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95371584..95372357hg38UCSC Ensembl
Innerchr11:95371589..95372352hg38UCSC Ensembl
Outerchr11:95371579..95372362hg38UCSC Ensembl
chr11:95104748..95105521hg19UCSC Ensembl
Innerchr11:95104753..95105516hg19UCSC Ensembl
Outerchr11:95104743..95105526hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38774
hg19774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14243461, essv14243466, essv14243481, essv14243470, essv14243467, essv14243482, essv14243483, essv14243477, essv14243478, essv14243474, essv14243471, essv14243462, essv14243464, essv14243479, essv14243463, essv14243475, essv14243476, essv14243472, essv14243480, essv14243465, essv14243469, essv14243468, essv14243460, essv14243473
SamplesNA19700, HG04096, HG04222, HG04229, HG04202, NA21100, NA21092, HG03607, HG03941, NA20864, HG03667, HG04100, HG03754, NA20850, HG03976, HG03873, HG03750, HG04180, HG04186, HG03949, HG02790, HG04015, HG03977, HG03998
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627346
Frequency
Sample Size2504
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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