A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819234



Internal ID15237199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:169690753..169690960hg38UCSC Ensembl
Innerchr1:169659894..169660101hg19UCSC Ensembl
Innerchr1:167926518..167926725hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38208
hg19208
hg18208
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419170
SamplesAK1
Known GenesSELL
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)nsv819234
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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