A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1673275



Internal ID15184097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101783816..101882585hg38UCSC Ensembl
Innerchr15:102324019..102422788hg19UCSC Ensembl
Innerchr15:100141542..100240311hg18UCSC Ensembl
Innerchr15:100059283..100158052hg16UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3898770
hg1998770
hg1898770
hg1698770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469527
Supporting Variants
Samples
Known GenesOR4F13P, OR4F15, OR4F6
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)nssv1673275
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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