A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1418893



Internal ID15235947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196936635..196936996hg38UCSC Ensembl
Innerchr3:196663506..196663867hg19UCSC Ensembl
Innerchr3:198147903..198148264hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38362
hg19362
hg18362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819558
Supporting Variants
SamplesAK1
Known GenesNCBP2
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)nssv1418893
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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