A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662119



Internal ID2895206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112022547..112024925hg38UCSC Ensembl
chr11:111893271..111895649hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg382379
hg192379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6571063
SamplesNA19379
Known GenesDIXDC1, DLAT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662119
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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