A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9404



Internal ID15500630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:22373335..22375533hg38UCSC Ensembl
Outerchr16:22384656..22386854hg19UCSC Ensembl
Outerchr16:22292157..22294355hg18UCSC Ensembl
Outerchr16:22292157..22294355hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg382199
hg192199
hg182199
hg172199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22668, nssv26698
SamplesNA18860, NA18564
Known GenesCDR2
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)nsv9404
Frequency
Sample Size31
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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