A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469563



Internal ID15187592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89545246..89723819hg38UCSC Ensembl
Innerchr9:92160161..92338734hg19UCSC Ensembl
Innerchr9:91349981..91528554hg18UCSC Ensembl
Innerchr9:87651569..87830142hg16UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38178574
hg19178574
hg18178574
hg16178574
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1676417
Samples
Known GenesGADD45G, UNQ6494
MethodBAC aCGH
AnalysisA locus was considered a CNV if the log ratio of fluorescence measurements for the individuals assayed exceeded twice the SD of the autosomal clones in both dye-swapped experiments.
PlatformGPL4010
Comments
ReferenceLocke_et_al_2006
Pubmed ID16826518
Accession Number(s)nsv469563
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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