A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666961



Internal ID9933066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2162226..2163040hg38UCSC Ensembl
chr16:2212227..2213041hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38815
hg19815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6237853, essv5949102, essv6007632, essv5935108
SamplesHG00318, HG00346, HG00369, HG00323
Known GenesTRAF7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666961
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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