A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1672829



Internal ID15530337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:25500014..25647577hg38UCSC Ensembl
InnerchrY:27646161..27793724hg19UCSC Ensembl
InnerchrY:26055549..26203112hg18UCSC Ensembl
InnerchrY:26502195..26649758hg16UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg38147564
hg19147564
hg18147564
hg16147564
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469828
Supporting Variants
Samples
Known GenesCDY1, CDY1B
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)nssv1672829
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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