A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819104



Internal ID15237069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24843005..24843449hg38UCSC Ensembl
Innerchr6:24843233..24843677hg19UCSC Ensembl
Innerchr6:24951212..24951656hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38445
hg19445
hg18445
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418954
SamplesAK1
Known GenesFAM65B
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)nsv819104
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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