A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663939



Internal ID9930044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16768991..16770572hg38UCSC Ensembl
chr11:16790538..16792119hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381582
hg191582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6227989, essv5943284, essv6271188
SamplesNA18543, HG00473, NA18612
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663939
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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