A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678884



Internal ID9944989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117404104..117412628hg38UCSC Ensembl
chr11:117274820..117283344hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg388525
hg198525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6134391
SamplesHG01198
Known GenesCEP164
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678884
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer