A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663044



Internal ID9929149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1807027..1811541hg38UCSC Ensembl
Outerchr11:1806990..1811591hg38UCSC Ensembl
Innerchr11:1828257..1832771hg19UCSC Ensembl
Outerchr11:1828220..1832821hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384602
hg194602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6166137, essv5685595
SamplesNA18519, NA19436
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663044
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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