A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv550097



Internal ID15213791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:12197854..12365053hg38UCSC Ensembl
InnerchrY:14318560..14485784hg19UCSC Ensembl
InnerchrY:12828560..12995792hg18UCSC Ensembl
InnerchrY:13327831..13495063hg16UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38167200
hg19167225
hg18167233
hg16167233
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv471609
Supporting Variants
SamplesNA17017
Known Genes
MethodBAC aCGH
AnalysisArray image analysis and normalization were performed using UCSF Spot and Sproc software (Jain et al. 2002). BACs for which only one of the triplicates printed on the array yielded data, or for which the standard deviation of log2 ratio for the triplicates was 10.2, were removed from final analysis. Furthermore, we discarded BACs that failed to yield data in <20% of cases. For each hybridization experiment, we established a threshold log2 ratio of 2 SDs from the mean of all autosomal clones, and BACs that exceeded this threshold in both independent dye-swap experiments were classified as variant.
PlatformGPL4010
Comments
ReferenceSharp_et_al_2005
Pubmed ID15918152
Accession Number(s)nssv550097
Frequency
Sample Size48
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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