A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662596



Internal ID9928701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65249995..65257523hg38UCSC Ensembl
chr11:65017466..65024994hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387529
hg197529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5971332, essv5656031
SamplesNA19657, NA19786
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662596
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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