A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9905



Internal ID15847817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:38895828..38906550hg38UCSC Ensembl
Outerchr22:39291833..39302555hg19UCSC Ensembl
Outerchr22:37621779..37632501hg18UCSC Ensembl
Outerchr22:37616333..37627055hg17UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3810723
hg1910723
hg1810723
hg1710723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25922, nssv26306, nssv27948, nssv24853, nssv27371, nssv22980, nssv22595, nssv26160, nssv23009, nssv25391
SamplesNA11830, NA18980, NA07029, NA12155, NA12802, NA10839, NA10847, NA10863, NA12872, NA18972
Known Genes
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)nsv9905
Frequency
Sample Size31
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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