A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469761



Internal ID15187790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41586913..41747161hg38UCSC Ensembl
Innerchr9:46287855..46454477hg19UCSC Ensembl
Innerchr9:46177851..46344473hg18UCSC Ensembl
Innerchr9:43553553..43720175hg16UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38160249
hg19166623
hg18166623
hg16166623
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1672838, nssv1676523, nssv1672696, nssv1676052
Samples
Known GenesFAM27E1
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)nsv469761
Frequency
Sample Size265
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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