A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676366



Internal ID9595785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57011511..57014247hg38UCSC Ensembl
Outerchr16:57011474..57014297hg38UCSC Ensembl
Innerchr16:57045423..57048159hg19UCSC Ensembl
Outerchr16:57045386..57048209hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg382824
hg192824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6299867
SamplesNA19901
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676366
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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