A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673699



Internal ID9593118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120129631..120131723hg38UCSC Ensembl
chr11:120000339..120002431hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382093
hg192093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5517090
SamplesHG00581
Known GenesTRIM29
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673699
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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