A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663211



Internal ID9929316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56616788..56627870hg38UCSC Ensembl
Outerchr11:56616751..56627920hg38UCSC Ensembl
Innerchr11:56384264..56395346hg19UCSC Ensembl
Outerchr11:56384227..56395396hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3811170
hg1911170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6240058
SamplesNA20522
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663211
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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