A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819618



Internal ID15237583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141778191..141779075hg38UCSC Ensembl
Innerchr3:141497033..141497917hg19UCSC Ensembl
Innerchr3:142979723..142980607hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38885
hg19885
hg18885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419107
SamplesAK1
Known GenesGRK7
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)nsv819618
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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