A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819466



Internal ID15584167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151478846..151502178hg38UCSC Ensembl
Innerchr3:151196634..151219966hg19UCSC Ensembl
Innerchr3:152679324..152702656hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3823333
hg1923333
hg1823333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418690
SamplesAK1
Known Genes
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)nsv819466
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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