A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659832



Internal ID9925937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66701974..66705031hg38UCSC Ensembl
chr16:66735877..66738934hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg383058
hg193058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6567967, essv5823257, essv5505906, essv6083536, essv6288034, essv6216860, essv5840831, essv5805178, essv6541799, essv5678097, essv5909380, essv5986695, essv6173432, essv6205265, essv5605017, essv6155576, essv5670854, essv5537465, essv6241093, essv6494834, essv5744578, essv6158783, essv5613694, essv5923937, essv6422962, essv5726687, essv5492616, essv6036540, essv5888110, essv5592444, essv5838297, essv5960396, essv5627137, essv6450255, essv6376748, essv5711859, essv6475824, essv5592542
SamplesNA18924, NA19909, NA19704, NA19355, NA19819, NA18504, NA19190, NA18510, NA19119, NA18916, NA19197, NA19313, NA19207, NA19159, NA19189, NA19239, NA18908, NA19985, NA18867, HG01183, NA19908, NA19247, NA19437, NA19152, NA19236, NA18516, NA19982, NA18499, NA18853, NA19452, NA19108, NA19147, NA19712, NA19434, NA19444, NA19331, NA19240, NA19900
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659832
Frequency
Sample Size1151
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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