A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469880



Internal ID15534595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:26445618..26584064hg38UCSC Ensembl
InnerchrY:28591765..28730211hg19UCSC Ensembl
InnerchrY:27001153..27139599hg18UCSC Ensembl
InnerchrY:27514763..27653209hg16UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg38138447
hg19138447
hg18138447
hg16138447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1676004
Samples
Known Genes
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)nsv469880
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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