A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1673655



Internal ID15184477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42469682..42682875hg38UCSC Ensembl
Innerchr10:42965130..43178323hg19UCSC Ensembl
Innerchr10:42285136..42498329hg18UCSC Ensembl
Innerchr10:42249136..42462329hg16UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38213194
hg19213194
hg18213194
hg16213194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469725
Supporting Variants
Samples
Known GenesCCNYL2, LINC00839, ZNF33B, ZNF37BP
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)nssv1673655
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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