A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1673039



Internal ID15530547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41629654..41736086hg38UCSC Ensembl
Innerchr9:46298863..46405393hg19UCSC Ensembl
Innerchr9:46188859..46295389hg18UCSC Ensembl
Innerchr9:43564561..43671091hg16UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38106433
hg19106531
hg18106531
hg16106531
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469535
Supporting Variants
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)nssv1673039
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