A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419205



Internal ID15236259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20245723..20246950hg38UCSC Ensembl
Innerchr8:20103234..20104461hg19UCSC Ensembl
Innerchr8:20147514..20148741hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg381228
hg191228
hg181228
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819988
Supporting Variants
SamplesAK1
Known GenesLZTS1
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)nssv1419205
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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