A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658274



Internal ID9924379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65874145..65876851hg38UCSC Ensembl
Outerchr11:65873774..65877221hg38UCSC Ensembl
Innerchr11:65641616..65644322hg19UCSC Ensembl
Outerchr11:65641245..65644692hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383448
hg193448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6284294, essv5986167, essv6408729, essv6419183
SamplesHG01518, HG01519, HG01515, HG01516
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658274
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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