A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678883



Internal ID9944988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47380009..47381602hg38UCSC Ensembl
chr11:47401560..47403153hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381594
hg191594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6135093
SamplesNA20289
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678883
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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