A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419814



Internal ID15236868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:38907812..38908108hg38UCSC Ensembl
Innerchr19:39398452..39398748hg19UCSC Ensembl
Innerchr19:44090292..44090588hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38297
hg19297
hg18297
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv820174
Supporting Variants
SamplesAK1
Known GenesNFKBIB
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)nssv1419814
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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