A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2045841



Internal ID7716952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:164840172..164840576hg38UCSC Ensembl
Outerchr2:164839999..164840731hg38UCSC Ensembl
Innerchr2:165696682..165697086hg19UCSC Ensembl
Outerchr2:165696509..165697241hg19UCSC Ensembl
Innerchr2:165404928..165405332hg18UCSC Ensembl
Outerchr2:165404755..165405487hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38733
hg19733
hg18733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4667581
SamplesNA18507
Known GenesCOBLL1
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)esv2045841
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer