A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666803



Internal ID9586222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131630103..131630635hg38UCSC Ensembl
chr11:131499997..131500529hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6404892, essv5997715, essv5480664, essv5931678
SamplesNA18973, HG00662, NA19080, NA19065
Known GenesNTM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666803
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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