A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819062



Internal ID15237027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:89010401..89013391hg38UCSC Ensembl
Innerchr1:89476084..89479074hg19UCSC Ensembl
Innerchr1:89248672..89251662hg18UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg382991
hg192991
hg182991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419497
SamplesAK1
Known GenesGBP3
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)nsv819062
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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