A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672892



Internal ID9592311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66487242..66488760hg38UCSC Ensembl
chr16:66521145..66522663hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381519
hg191519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5844620
SamplesNA19452
Known GenesBEAN1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672892
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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