A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419395



Internal ID15236449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:133419150..133421301hg38UCSC Ensembl
Innerchr3:133137994..133140145hg19UCSC Ensembl
Innerchr3:134620684..134622835hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382152
hg192152
hg182152
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819235
Supporting Variants
SamplesAK1
Known GenesBFSP2
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)nssv1419395
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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