A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419244



Internal ID15236298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:168108953..168110311hg38UCSC Ensembl
Innerchr4:169030104..169031462hg19UCSC Ensembl
Innerchr4:169266679..169268037hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg381359
hg191359
hg181359
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv820236
Supporting Variants
SamplesAK1
Known GenesANXA10
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)nssv1419244
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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