A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv491n67



Internal ID20147003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75504544..75546815hg38UCSC Ensembl
chr16:75538442..75580713hg19UCSC Ensembl
chr16:74095943..74138214hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3842272
hg1942272
hg1842272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv827750, nsv827748, nsv827749
SamplesNA18951, NA18566, NA18997
Known GenesCHST5, TMEM231
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)dgv491n67
Frequency
Sample Size31
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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