A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658913



Internal ID9578332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89124386..89131303hg38UCSC Ensembl
Outerchr16:89124349..89131353hg38UCSC Ensembl
Innerchr16:89190794..89197711hg19UCSC Ensembl
Outerchr16:89190757..89197761hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg387005
hg197005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5773284, essv5961630
SamplesNA20795, NA20797
Known GenesACSF3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658913
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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