A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627690



Internal ID7014518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108931729..108933404hg38UCSC Ensembl
Innerchr11:108931729..108933404hg38UCSC Ensembl
Outerchr11:108931473..108933660hg38UCSC Ensembl
chr11:108802456..108804131hg19UCSC Ensembl
Innerchr11:108802456..108804131hg19UCSC Ensembl
Outerchr11:108802200..108804387hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381676
hg191676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14278462, essv14278482, essv14278487, essv14278467, essv14278472, essv14278477, essv14278476, essv14278470, essv14278483, essv14278461, essv14278474, essv14278464, essv14278471, essv14278478, essv14278475, essv14278465, essv14278466, essv14278459, essv14278481, essv14278458, essv14278484, essv14278480, essv14278460, essv14278486, essv14278479, essv14278469, essv14278485, essv14278463, essv14278473, essv14278468, essv14278457
SamplesNA19700, HG03121, NA18924, HG03175, HG02318, NA18917, HG02888, NA19190, HG01070, HG03212, NA20340, NA19238, NA18864, HG03270, NA19908, HG03575, HG02968, HG03311, HG02429, NA18853, HG02979, HG02256, NA19225, HG02594, NA18501, NA20348, HG03279, HG02938, NA19093, HG01082, NA19346
Known GenesDDX10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627690
Frequency
Sample Size2504
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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