A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5788114



Internal ID8765517
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 Flag1
Merged StatusS
Merged Variantsesv2660459
Supporting Variants
SamplesNA19920
Known GenesITFG3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5788114
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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