A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9262



Internal ID15500488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:45094755..45097181hg38UCSC Ensembl
Outerchr15:45386953..45389379hg19UCSC Ensembl
Outerchr15:43174245..43176671hg18UCSC Ensembl
Outerchr15:43174245..43176671hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg382427
hg192427
hg182427
hg172427
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22950
SamplesNA12740
Known GenesDUOX2
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)nsv9262
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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