A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819644



Internal ID15237609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:9817550..9818201hg38UCSC Ensembl
Innerchr3:9859234..9859885hg19UCSC Ensembl
Innerchr3:9834234..9834885hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38652
hg19652
hg18652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419041
SamplesAK1
Known GenesARPC4-TTLL3, TTLL3
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)nsv819644
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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