A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1983545



Internal ID7654656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:58163403..58163478hg38UCSC Ensembl
Outerchr8:58163201..58163670hg38UCSC Ensembl
Innerchr8:59075962..59076037hg19UCSC Ensembl
Outerchr8:59075760..59076229hg19UCSC Ensembl
Innerchr8:59238516..59238591hg18UCSC Ensembl
Outerchr8:59238314..59238783hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38470
hg19470
hg18470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4892520
SamplesNA18507
Known Genes
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)esv1983545
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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