A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668607



Internal ID9934712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46395217..46465150hg38UCSC Ensembl
Outerchr16:46395183..46465185hg38UCSC Ensembl
Innerchr16:46429129..46499062hg19UCSC Ensembl
Outerchr16:46429095..46499097hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3870003
hg1970003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv494e199
Supporting Variantsessv6418050, essv5757656
SamplesHG01070, HG01061
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668607
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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