A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1916461



Internal ID7246429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:42988620..42988669hg38UCSC Ensembl
Outerchr8:42988441..42988853hg38UCSC Ensembl
Innerchr8:42843763..42843812hg19UCSC Ensembl
Outerchr8:42843584..42843996hg19UCSC Ensembl
Innerchr8:42962920..42962969hg18UCSC Ensembl
Outerchr8:42962741..42963153hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38413
hg19413
hg18413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4544682
SamplesNA18507
Known GenesHOOK3
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)esv1916461
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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