A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678418



Internal ID9597837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69969687..69976248hg38UCSC Ensembl
chr11:69815793..69822354hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg386562
hg196562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5794950, essv6365176
SamplesHG01440, HG01124
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678418
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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