A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv482149



Internal ID8548344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:102065390..102068035hg38UCSC Ensembl
Outerchr10:103825147..103827792hg19UCSC Ensembl
Outerchr10:103815137..103817782hg18UCSC Ensembl
Outerchr10:103815137..103817782hg17UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg382646
hg192646
hg182646
hg172646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv558510
SamplesKB1
Known GenesHPS6
MethodSequencing
AnalysisWe constructed duplication maps for the KB1 genome and estimated the absolute copy number of each duplication interval larger than 20 kb in length. Using absolute estimates of copy number, we calculated an in silico log2 ratio for each the KB1 genome and compared copy number predictions with previously published copy numbers detected in NA18507 and YH genomes.
PlatformIllumina Genome Analyzer and Roche/454 sequencer. For arrayCGH validation experiments we used Nimblegen
CommentsHPS6
ReferenceSchuster_et_al_2010
Pubmed ID20164927
Accession Number(s)nsv482149
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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