A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8444



Internal ID15846356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:33792374..33807433hg38UCSC Ensembl
Outerchr9:33792372..33807431hg19UCSC Ensembl
Outerchr9:33782372..33797431hg18UCSC Ensembl
Outerchr9:33782372..33797431hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3815060
hg1915060
hg1815060
hg1715060
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974, nssv17575, nssv17535, nssv17536, nssv16916
SamplesNA18980, NA18975, NA19007, NA18537, NA18552
Known GenesPRSS3
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)nsv8444
Frequency
Sample Size31
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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