A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1963605



Internal ID7634717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2657050..2657091hg38UCSC Ensembl
Outerchr5:2656863..2657274hg38UCSC Ensembl
Innerchr5:2657164..2657205hg19UCSC Ensembl
Outerchr5:2656977..2657388hg19UCSC Ensembl
Innerchr5:2710164..2710205hg18UCSC Ensembl
Outerchr5:2709977..2710388hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38412
hg19412
hg18412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4850978
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)esv1963605
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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