A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627966



Internal ID7014791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123808256..123811084hg38UCSC Ensembl
Innerchr11:123808261..123811080hg38UCSC Ensembl
Outerchr11:123808252..123811089hg38UCSC Ensembl
chr11:123678964..123681792hg19UCSC Ensembl
Innerchr11:123678969..123681788hg19UCSC Ensembl
Outerchr11:123678960..123681797hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg382829
hg192829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14301554, essv14301570, essv14301565, essv14301556, essv14301555, essv14301557, essv14301559, essv14301560, essv14301564, essv14301562, essv14301551, essv14301567, essv14301569, essv14301552, essv14301568, essv14301561, essv14301566, essv14301553, essv14301563, essv14301558
SamplesHG01985, HG02610, HG02583, HG03518, HG03074, NA19238, HG02716, HG01248, HG02511, NA19327, HG01989, NA18910, NA18907, HG02557, NA19376, HG03112, HG02053, HG02013, NA19121, HG01082
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627966
Frequency
Sample Size2504
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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