A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659168



Internal ID9925273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:115388823..115392068hg38UCSC Ensembl
Outerchr11:115388786..115392118hg38UCSC Ensembl
Innerchr11:115259541..115262786hg19UCSC Ensembl
Outerchr11:115259504..115262836hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383333
hg193333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6274805
SamplesNA20525
Known GenesCADM1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659168
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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