A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819527



Internal ID15237492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192270904..192278983hg38UCSC Ensembl
Innerchr3:191988693..191996772hg19UCSC Ensembl
Innerchr3:193471387..193479466hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg388080
hg198080
hg188080
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419855
SamplesAK1
Known GenesFGF12
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)nsv819527
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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