A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9670



Internal ID15847582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:15649504..15665950hg38UCSC Ensembl
Outerchr19:15760314..15776760hg19UCSC Ensembl
Outerchr19:15621314..15637760hg18UCSC Ensembl
Outerchr19:15621314..15637760hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3816447
hg1916447
hg1816447
hg1716447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21640
SamplesNA12802
Known GenesCYP4F3
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)nsv9670
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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