A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9451



Internal ID15500677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:59601336..59998937hg38UCSC Ensembl
Outerchr16:59635240..60032841hg19UCSC Ensembl
Outerchr16:58192741..58590342hg18UCSC Ensembl
Outerchr16:58192741..58590342hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38397602
hg19397602
hg18397602
hg17397602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22494
SamplesNA18975
Known GenesAPOOP5
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)nsv9451
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