A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672179



Internal ID9938284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:115788942..115790121hg38UCSC Ensembl
Outerchr11:115788905..115790171hg38UCSC Ensembl
Innerchr11:115659660..115660839hg19UCSC Ensembl
Outerchr11:115659623..115660889hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381267
hg191267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5833993
SamplesNA18916
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672179
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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