A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419420



Internal ID15236474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:52785718..52788066hg38UCSC Ensembl
Innerchr14:53252436..53254784hg19UCSC Ensembl
Innerchr14:52322186..52324534hg18UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg382349
hg192349
hg182349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819339
Supporting Variants
SamplesAK1
Known GenesGNPNAT1
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)nssv1419420
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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