A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419736



Internal ID15236790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:57009876..57010164hg38UCSC Ensembl
Innerchr12:57403660..57403948hg19UCSC Ensembl
Innerchr12:55689927..55690215hg18UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv820171
Supporting Variants
SamplesAK1
Known GenesTAC3
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)nssv1419736
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer