A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819931



Internal ID15584632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:70286111..70288194hg38UCSC Ensembl
Innerchr18:67953347..67955430hg19UCSC Ensembl
Innerchr18:66104327..66106410hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg382084
hg192084
hg182084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419383
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)nsv819931
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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