A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819719



Internal ID15237684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89406006..89414843hg38UCSC Ensembl
Innerchr10:91165763..91174600hg19UCSC Ensembl
Innerchr10:91155743..91164580hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg388838
hg198838
hg188838
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418557
SamplesAK1
Known GenesIFIT1, IFIT5
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)nsv819719
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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