A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469720



Internal ID15187749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14865281..15037379hg38UCSC Ensembl
Innerchr10:14907280..15079378hg19UCSC Ensembl
Innerchr10:14947286..15119384hg18UCSC Ensembl
Innerchr10:14911286..15083384hg16UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38172099
hg19172099
hg18172099
hg16172099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1672986
Samples
Known GenesDCLRE1C, HSPA14, MEIG1, SUV39H2
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)nsv469720
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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