A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9479



Internal ID15500705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89878586..89880246hg38UCSC Ensembl
Outerchr16:89944994..89946654hg19UCSC Ensembl
Outerchr16:88472495..88474155hg18UCSC Ensembl
Outerchr16:88472495..88474155hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381661
hg191661
hg181661
hg171661
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25293
SamplesNA12155
Known GenesTCF25
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)nsv9479
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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