A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2233361



Internal ID7904472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241566691..241567965hg38UCSC Ensembl
Outerchr2:241566567..241568125hg38UCSC Ensembl
Innerchr2:242506106..242507380hg19UCSC Ensembl
Outerchr2:242505982..242507540hg19UCSC Ensembl
Innerchr2:242154779..242156053hg18UCSC Ensembl
Outerchr2:242154655..242156213hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381559
hg191559
hg181559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4846175
SamplesNA18507
Known GenesBOK
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)esv2233361
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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