A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663468



Internal ID9929573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14429588..14442764hg38UCSC Ensembl
Outerchr11:14429431..14442917hg38UCSC Ensembl
Innerchr11:14451134..14464310hg19UCSC Ensembl
Outerchr11:14450977..14464463hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3813487
hg1913487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5532494
SamplesHG00701
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663468
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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