A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv482098



Internal ID15234571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:113857348..113863475hg38UCSC Ensembl
Outerchr6:114178527..114184652hg19UCSC Ensembl
Outerchr6:114285220..114291345hg18UCSC Ensembl
Outerchr6:114285220..114291345hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386128
hg196126
hg186126
hg176126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv558459
SamplesKB1
Known GenesMARCKS
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
CommentsMARCKS
ReferenceSchuster_et_al_2010
Pubmed ID20164927
Accession Number(s)nsv482098
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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