A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv549310



Internal ID15214079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89545247..89723819hg38UCSC Ensembl
Innerchr9:92160162..92338734hg19UCSC Ensembl
Innerchr9:91349982..91528554hg18UCSC Ensembl
Innerchr9:87651570..87830142hg16UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38178573
hg19178573
hg18178573
hg16178573
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv471662
Supporting Variants
SamplesNA17059
Known GenesGADD45G, UNQ6494
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)nssv549310
Frequency
Sample Size48
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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