A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668036



Internal ID9587455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13962055..14027138hg38UCSC Ensembl
chr11:13983602..14048685hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3865084
hg1965084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5946308, essv6456959
SamplesHG00657, HG00702
Known GenesSPON1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668036
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