A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419293



Internal ID15583077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:205530018..205531638hg38UCSC Ensembl
Innerchr1:205499146..205500766hg19UCSC Ensembl
Innerchr1:203765769..203767389hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381621
hg191621
hg181621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv820091
Supporting Variants
SamplesAK1
Known GenesCDK18
MethodOligo aCGH
AnalysisThe array was scanned with Agilent DNA microarray scanner at 2 micron resolution. The resulting image was extracted by Agilent's Feature Extraction software. The log2 ratios were analyzed using NEXUS software. Each aberration call was manually checked to confirm the accuracy of the calls.
PlatformGSE19651
Comments
ReferenceKim_et_al_2009
Pubmed ID19587683
Accession Number(s)nssv1419293
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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