A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469834



Internal ID15187863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:13874062..14015947hg38UCSC Ensembl
InnerchrY:15985942..16127827hg19UCSC Ensembl
InnerchrY:14495336..14637221hg18UCSC Ensembl
InnerchrY:14994607..15136492hg16UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg38141886
hg19141886
hg18141886
hg16141886
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1676309
Samples
Known GenesVCY, VCY1B
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)nsv469834
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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