A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1673164



Internal ID15530672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31922243..32111643hg38UCSC Ensembl
Innerchr15:32214446..32403844hg19UCSC Ensembl
Innerchr15:30001738..30191136hg18UCSC Ensembl
Innerchr15:29930502..30119900hg16UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38189401
hg19189399
hg18189399
hg16189399
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469870
Supporting Variants
Samples
Known GenesCHRNA7
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)nssv1673164
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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