A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660728



Internal ID9926833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5476751..5477271hg38UCSC Ensembl
chr11:5497981..5498501hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6586523, essv6034733, essv5858712, essv6298916, essv5708127, essv5403340, essv5827055
SamplesHG00608, HG00610, HG00583, HG00473, NA19080, NA18552, NA19074
Known GenesOR51B5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660728
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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