A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv834143



Internal ID16458012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:21163703..21314316hg38UCSC Ensembl
Outerchr22:21517992..21668605hg19UCSC Ensembl
Outerchr22:19847992..19998605hg18UCSC Ensembl
Outerchr22:19842546..19993159hg17UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38150614
hg19150614
hg18150614
hg17150614
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1455769, nssv1455737, nssv1455771, nssv1455735, nssv1455741, nssv1455764, nssv1455756, nssv1455767, nssv1455766, nssv1455768, nssv1455728, nssv1455787, nssv1455783, nssv1455774, nssv1455750, nssv1455765, nssv1455730, nssv1455734, nssv1455748, nssv1455760, nssv1455753, nssv1455745, nssv1455759, nssv1455742, nssv1455776, nssv1455785, nssv1455790, nssv1455739, nssv1455780, nssv1455788, nssv1455751, nssv1455778, nssv1455772, nssv1455773, nssv1455738, nssv1455789, nssv1455736, nssv1455761, nssv1455729, nssv1455779, nssv1455749, nssv1455754, nssv1455781, nssv1455777, nssv1455786, nssv1455752, nssv1455740, nssv1455784, nssv1455743, nssv1455762, nssv1455744, nssv1455770, nssv1455755, nssv1455731, nssv1455747, nssv1455763, nssv1455757, nssv1455791, nssv1455732, nssv1455775, nssv1455758, nssv1455746, nssv1455782, nssv1455733
Samples
Known GenesFAM230B, POM121L8P
MethodBAC aCGH
AnalysisExperimental SDs (SDautosome) were calculated for each experiment on the basis of the log2 ratios of the 24,392 reliable clones minus the clones removed because of low signal-to-noise ratio (SNR) or high SD of replicate clone measures (SDclone). Thresholds for determining CNV clones were set at a multiple of the SDautosome value. For each experiment, clones were annotated as uninformative if they were filtered via SNR or SDclone, as a CNV loss if the log2 ratio was less than the negative threshold, as unchanged if the log2 ratio was between the negative and positive thresholds, and as a CNV gain if the log2 ratio was above the positive threshold.
PlatformGPL2616
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv834143
Frequency
Sample Size95
Observed Gain63
Observed Loss1
Observed Complex0
Frequencyn/a


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