A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671246



Internal ID9937351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118862540..118862710hg38UCSC Ensembl
chr11:118733249..118733419hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5754004, essv6212042, essv5738339, essv5803892, essv6137816, essv5654143, essv6327706, essv5688918, essv6302649, essv5847234, essv6515952, essv5580969, essv6560641, essv6237747, essv5752187, essv5672918, essv6308642, essv5551644, essv5407412, essv6252126, essv6258673, essv5716673, essv5626987, essv5537035, essv6311178
SamplesNA19397, NA19377, NA20356, NA18510, NA19381, NA19379, NA19382, NA19404, NA19317, HG01048, NA18871, HG01149, HG01073, NA19395, NA19401, NA18517, NA19380, HG01108, NA19360, NA18501, NA19770, NA19316, NA19312, NA20322, NA18511
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671246
Frequency
Sample Size1151
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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