A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659996



Internal ID9926101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92291526..92294811hg38UCSC Ensembl
chr11:92024692..92027977hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg383286
hg193286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv233e199
Supporting Variantsessv5750823, essv6578549, essv6116904, essv6323796, essv6423227
SamplesHG00318, HG00251, NA20342, HG00250, HG00310
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659996
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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