A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469653



Internal ID15534368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38650705..38839549hg38UCSC Ensembl
Innerchr10:38943836..39132680hg19UCSC Ensembl
Innerchr10:38983842..39172686hg18UCSC Ensembl
Innerchr10:38947842..39136686hg16UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38188845
hg19188845
hg18188845
hg16188845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1674369
Samples
Known GenesACTR3BP5
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)nsv469653
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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