A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661599



Internal ID9581018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67139916..67149786hg38UCSC Ensembl
Outerchr11:67139759..67149939hg38UCSC Ensembl
Innerchr11:66907387..66917257hg19UCSC Ensembl
Outerchr11:66907230..66917410hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3810181
hg1910181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6306018, essv5966184, essv5458623, essv6182676, essv5979798, essv5496368
SamplesHG00269, NA11894, HG00232, HG00367, HG00324, HG00312
Known GenesKDM2A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661599
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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