A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819220



Internal ID15237185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:42575615..42575754hg38UCSC Ensembl
Innerchr4:42577632..42577771hg19UCSC Ensembl
Innerchr4:42272389..42272528hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38140
hg19140
hg18140
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419214
SamplesAK1
Known GenesATP8A1
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)nsv819220
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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