A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2122305



Internal ID7793416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:4866435..4866515hg38UCSC Ensembl
Outerchr5:4866265..4866678hg38UCSC Ensembl
Innerchr5:4866548..4866628hg19UCSC Ensembl
Outerchr5:4866378..4866791hg19UCSC Ensembl
Innerchr5:4919548..4919628hg18UCSC Ensembl
Outerchr5:4919378..4919791hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38414
hg19414
hg18414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4644859
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)esv2122305
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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