A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669056



Internal ID9935161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45822714..45823851hg38UCSC Ensembl
chr11:45844265..45845402hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381138
hg191138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6530554, essv5879218, essv5641656, essv6565661, essv5753888, essv5538609, essv6586530, essv5448099, essv6461216, essv6422168, essv6419674, essv6025600, essv5951982, essv5922672, essv5855293, essv6116671
SamplesNA19664, NA11933, NA20816, HG01167, HG01083, HG00277, HG00232, NA20515, NA10847, NA20804, NA20527, NA20778, NA20510, HG00252, NA20503, NA20502
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669056
Frequency
Sample Size1151
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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