A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667389



Internal ID9933494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65436488..65443581hg38UCSC Ensembl
Outerchr11:65436451..65443631hg38UCSC Ensembl
Innerchr11:65203959..65211052hg19UCSC Ensembl
Outerchr11:65203922..65211102hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387181
hg197181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6444617
SamplesHG00231
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667389
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