A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666963



Internal ID9933068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102878570..102882598hg38UCSC Ensembl
Outerchr11:102878413..102882751hg38UCSC Ensembl
Innerchr11:102749300..102753328hg19UCSC Ensembl
Outerchr11:102749143..102753481hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg384339
hg194339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6302314
SamplesHG00442
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666963
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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