A curated catalogue of human genomic structural variation

Variant Details

Variant: nsv824524

Internal ID16086998
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7802093..7930063hg38UCSC Ensembl
Innerchr8:7659615..7787585hg19UCSC Ensembl
Innerchr8:7697025..7824995hg18UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1427599, nssv1425882, nssv1441180, nssv1422714, nssv1434517, nssv1426809, nssv1436773
SamplesNA18570, NA18969, NA18542, AK8, AK4, NA18552, AK6
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4A, SPAG11A, SPAG11B, ZNF705B
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
Pubmed ID20364138
Accession Number(s)nsv824524
Sample Size31
Observed Gain5
Observed Loss2
Observed Complex0

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