A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv776n67



Internal ID20147288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:46021994..46096286hg38UCSC Ensembl
chr22:46417874..46492166hg19UCSC Ensembl
chr22:44796538..44870830hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3874293
hg1974293
hg1874293
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv829287, nsv829288, nsv829284
SamplesAK6, NA18949, NA18542
Known GenesC22orf26, LINC00899, LOC150381, MIR3619, MIRLET7BHG
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)dgv776n67
Frequency
Sample Size31
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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