A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469717



Internal ID15187746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:18077233..18240697hg38UCSC Ensembl
InnerchrY:20239119..20402583hg19UCSC Ensembl
InnerchrY:18698507..18861971hg18UCSC Ensembl
InnerchrY:19134303..19297767hg16UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg38163465
hg19163465
hg18163465
hg16163465
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1676295, nssv1672652
Samples
Known GenesXKRY, XKRY2
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)nsv469717
Frequency
Sample Size265
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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