A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8522



Internal ID15846434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69394356..69419819hg38UCSC Ensembl
Outerchr9:72009272..72034735hg19UCSC Ensembl
Outerchr9:71199092..71224555hg18UCSC Ensembl
Outerchr9:69238826..69264289hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3825464
hg1925464
hg1825464
hg1725464
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17794, nssv20991, nssv16331, nssv19238, nssv18517
SamplesNA11830, NA12155, NA18860, NA10839, NA12872
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)nsv8522
Frequency
Sample Size31
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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