A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9403



Internal ID15500629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:22189083..22200028hg38UCSC Ensembl
Outerchr16:22200404..22211349hg19UCSC Ensembl
Outerchr16:22107905..22118850hg18UCSC Ensembl
Outerchr16:22107905..22118850hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3810946
hg1910946
hg1810946
hg1710946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv27804
SamplesNA19221
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)nsv9403
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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