A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2233598



Internal ID7904709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35501508..35501633hg38UCSC Ensembl
Outerchr6:35501371..35501780hg38UCSC Ensembl
Innerchr6:35469285..35469410hg19UCSC Ensembl
Outerchr6:35469148..35469557hg19UCSC Ensembl
Innerchr6:35577263..35577388hg18UCSC Ensembl
Outerchr6:35577126..35577535hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38410
hg19410
hg18410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4765394
SamplesNA18507
Known GenesTULP1
MethodSequencing
AnalysisHierarchical clustering of anomalous readpairs was used to identify groupings of five or more readpairs that had a similar size and position. Read pairs were defined as anomalous if they had high-confidence alignments of each individual read that nevertheless were either incorrectly oriented or implied an insert size of at least 3 standard deviations outside the sample median.
PlatformNot specified
Comments
ReferenceBentley_et_al_2008
Pubmed ID18987734
Accession Number(s)esv2233598
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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