A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv482159



Internal ID15234632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:65354811..65357611hg38UCSC Ensembl
Outerchr11:65122282..65125082hg19UCSC Ensembl
Outerchr11:64878858..64881658hg18UCSC Ensembl
Outerchr11:64878858..64881658hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382801
hg192801
hg182801
hg172801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv558520
SamplesKB1
Known GenesTIGD3
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
CommentsTIGD3
ReferenceSchuster_et_al_2010
Pubmed ID20164927
Accession Number(s)nsv482159
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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