A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2123340



Internal ID7794451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:174265257..174265348hg38UCSC Ensembl
Outerchr4:174265096..174265494hg38UCSC Ensembl
Innerchr4:175186408..175186499hg19UCSC Ensembl
Outerchr4:175186247..175186645hg19UCSC Ensembl
Innerchr4:175422983..175423074hg18UCSC Ensembl
Outerchr4:175422822..175423220hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38399
hg19399
hg18399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4956802
SamplesNA18507
Known GenesFBXO8
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)esv2123340
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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