A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469854



Internal ID15534569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:26125132..26292559hg38UCSC Ensembl
InnerchrY:28271279..28438706hg19UCSC Ensembl
InnerchrY:26680667..26848094hg18UCSC Ensembl
InnerchrY:27194277..27361704hg16UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg38167428
hg19167428
hg18167428
hg16167428
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1673454, nssv1672412
Samples
Known Genes
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)nsv469854
Frequency
Sample Size265
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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