A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819568



Internal ID15584269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:98044332..98045856hg38UCSC Ensembl
Innerchr1:98509888..98511412hg19UCSC Ensembl
Innerchr1:98282476..98284000hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg381525
hg191525
hg181525
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419278
SamplesAK1
Known GenesMIR137HG, MIR2682
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)nsv819568
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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