A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1932815



Internal ID7593617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9989988..9990203hg38UCSC Ensembl
Outerchr5:9989812..9990381hg38UCSC Ensembl
Innerchr5:9990100..9990315hg19UCSC Ensembl
Outerchr5:9989924..9990493hg19UCSC Ensembl
Innerchr5:10043100..10043315hg18UCSC Ensembl
Outerchr5:10042924..10043493hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38570
hg19570
hg18570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4602772
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)esv1932815
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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