A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674186



Internal ID9593605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:111289712..111291895hg38UCSC Ensembl
Outerchr11:111289555..111292048hg38UCSC Ensembl
Innerchr11:111160437..111162620hg19UCSC Ensembl
Outerchr11:111160280..111162773hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg382494
hg192494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6229472
SamplesNA18623
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674186
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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