A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469695



Internal ID15534410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:21846590..22015423hg38UCSC Ensembl
InnerchrY:23992737..24161570hg19UCSC Ensembl
InnerchrY:22402125..22570958hg18UCSC Ensembl
InnerchrY:22837921..23006754hg16UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38168834
hg19168834
hg18168834
hg16168834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1676425
Samples
Known GenesRBMY1A1, RBMY1B, RBMY1D, RBMY1E
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)nsv469695
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