A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469635



Internal ID15187664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:21486585..21628623hg38UCSC Ensembl
InnerchrY:23648471..23790509hg19UCSC Ensembl
InnerchrY:22057859..22199897hg18UCSC Ensembl
InnerchrY:22493655..22635693hg16UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38142039
hg19142039
hg18142039
hg16142039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1674936
Samples
Known GenesRBMY1A1, RBMY1B, RBMY1D, RBMY1E, TTTY13
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)nsv469635
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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