A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9471



Internal ID15500697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:87881137..87941142hg38UCSC Ensembl
Outerchr16:87914743..87974748hg19UCSC Ensembl
Outerchr16:86472244..86532249hg18UCSC Ensembl
Outerchr16:86472244..86532249hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3860006
hg1960006
hg1860006
hg1760006
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26738, nssv28129
SamplesNA18517, NA19221
Known GenesCA5A
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)nsv9471
Frequency
Sample Size31
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer