A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1674022



Internal ID15531530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4312311..4453111hg38UCSC Ensembl
Innerchr11:4333541..4474341hg19UCSC Ensembl
Innerchr11:4290117..4430917hg18UCSC Ensembl
Innerchr11:4297850..4438650hg16UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38140801
hg19140801
hg18140801
hg16140801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469800
Supporting Variants
Samples
Known GenesOR52B4, OR52K2, TRIM21
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)nssv1674022
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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