A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469743



Internal ID15534458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:6183698..6334031hg38UCSC Ensembl
InnerchrY:6051739..6202072hg19UCSC Ensembl
InnerchrY:6111739..6262072hg18UCSC Ensembl
InnerchrY:5754695..5905028hg16UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38150334
hg19150334
hg18150334
hg16150334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv18n29
Supporting Variantsnssv1673369, nssv1672631
Samples
Known GenesTSPY2, TTTY23, TTTY23B
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)nsv469743
Frequency
Sample Size265
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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