A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676979



Internal ID9943084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39695176..39697381hg38UCSC Ensembl
chr11:39716726..39718931hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382206
hg192206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6002584, essv5729192, essv5534464, essv5688388, essv5626080, essv6549441, essv6212035, essv6511254, essv5609589, essv5955937
SamplesNA18999, NA18944, NA18960, NA18949, NA19002, NA18985, NA19007, NA19080, NA19429, NA19074
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676979
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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