A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819553



Internal ID15237518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24675585..24676525hg38UCSC Ensembl
Innerchr15:24920732..24921672hg19UCSC Ensembl
Innerchr15:22471825..22472765hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38941
hg19941
hg18941
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419130
SamplesAK1
Known GenesNPAP1
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)nsv819553
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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