A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1676295



Internal ID15187117
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 StatusS
Merged Variantsnsv469717
Supporting Variants
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)nssv1676295
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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