A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660459



Internal ID9579878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:244784..246872hg38UCSC Ensembl
chr16:294783..296871hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382089
hg192089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5788114
SamplesNA19920
Known GenesITFG3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660459
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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