A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670718



Internal ID9936823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:108209196..108217292hg38UCSC Ensembl
Outerchr11:108209159..108217342hg38UCSC Ensembl
Innerchr11:108079923..108088019hg19UCSC Ensembl
Outerchr11:108079886..108088069hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg388184
hg198184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6450899
SamplesHG00583
Known GenesNPAT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670718
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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