A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv826565



Internal ID16089039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132296460..132298590hg38UCSC Ensembl
Innerchr12:132873046..132875176hg19UCSC Ensembl
Innerchr12:131383119..131385249hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg382131
hg192131
hg182131
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1424511, nssv1436970
SamplesNA18542, NA18582
Known GenesGALNT9
MethodOligo aCGH
AnalysisTo select parameters for calling CNVs (that is, the statistical threshold of the ADM2 algorithm, the minimum +/- log2 ratio and the minimum number of consecutive probes in a CNV interval), we calculated the sensitivity and positive predictive value based on the comparison of aCGH-based CNV calls (using our high-resolution Agilent 24M platform) with read-depth sequence data for two samples from Korean individuals (AK1 and AK2). We attempted to obtain `absolute' copy number status of the sample from NA10851, which was used as the reference sample for aCGH experiments in this study. For this, we used read-depth data for NA10851 obtained from massively parallel sequencing by the Illumina GA II data. The read-depth data represent the copy number status of NA10851 as compared to the human reference genome (hg18) because the short read sequences were aligned to hg18.
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv826565
Frequency
Sample Size31
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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