A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4873125



Internal ID7458757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6036811..6037719hg38UCSC Ensembl
Outerchr4:6036733..6037772hg38UCSC Ensembl
Innerchr4:6038538..6039446hg19UCSC Ensembl
Outerchr4:6038460..6039499hg19UCSC Ensembl
Innerchr4:6089439..6090347hg18UCSC Ensembl
Outerchr4:6089361..6090400hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381040
hg191040
hg181040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2324557
Supporting Variants
SamplesNA18507
Known GenesJAKMIP1
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)essv4873125
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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