A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1675311



Internal ID15186133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101737032..101890871hg38UCSC Ensembl
Innerchr15:102277235..102431074hg19UCSC Ensembl
Innerchr15:100094758..100248597hg18UCSC Ensembl
Innerchr15:100012499..100166338hg16UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38153840
hg19153840
hg18153840
hg16153840
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469708
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)nssv1675311
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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