A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672242



Internal ID9938347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117933522..117939443hg38UCSC Ensembl
chr11:117804237..117810158hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385922
hg195922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5769393
SamplesHG00108
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672242
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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