A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819142



Internal ID15583843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70112001..70112207hg38UCSC Ensembl
Innerchr10:71871757..71871963hg19UCSC Ensembl
Innerchr10:71541763..71541969hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38207
hg19207
hg18207
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419181
SamplesAK1
Known GenesH2AFY2
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)nsv819142
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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