A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26579



Internal ID15487510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33859716..33861400hg38UCSC Ensembl
Outerchr16:33858932..33862046hg38UCSC Ensembl
Innerchr16:33662183..33663867hg19UCSC Ensembl
Outerchr16:33661399..33664513hg19UCSC Ensembl
Innerchr16:33569684..33571368hg18UCSC Ensembl
Outerchr16:33568900..33572014hg18UCSC Ensembl
Innerchr16:33569684..33571368hg17UCSC Ensembl
Outerchr16:33568900..33572014hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg383115
hg193115
hg183115
hg173115
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18517
Known Genes
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv26579
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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