A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678965



Internal ID9945070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36484987..36487126hg38UCSC Ensembl
chr11:36506537..36508676hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382140
hg192140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5949768, essv5827919, essv5722449, essv6269412, essv5702369
SamplesNA19703, NA19920, NA19904, NA19236, NA19711
Known GenesTRAF6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678965
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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