A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819521



Internal ID15237486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9338335..9338764hg38UCSC Ensembl
Innerchr19:9449011..9449440hg19UCSC Ensembl
Innerchr19:9310011..9310440hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38430
hg19430
hg18430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418950
SamplesAK1
Known GenesZNF559, ZNF559-ZNF177
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)nsv819521
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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