A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv827779



Internal ID16090253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83774879..83775451hg38UCSC Ensembl
Innerchr16:83808484..83809056hg19UCSC Ensembl
Innerchr16:82365985..82366557hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38573
hg19573
hg18573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv495n67
Supporting Variantsnssv1422995, nssv1435468, nssv1438481
SamplesNA18951, NA18942, NA18552
Known GenesCDH13
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)nsv827779
Frequency
Sample Size31
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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