A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2258950



Internal ID7930061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:172551672..172551788hg38UCSC Ensembl
Outerchr5:172551538..172551897hg38UCSC Ensembl
Innerchr5:171978675..171978791hg19UCSC Ensembl
Outerchr5:171978541..171978900hg19UCSC Ensembl
Innerchr5:171911280..171911396hg18UCSC Ensembl
Outerchr5:171911146..171911505hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38360
hg19360
hg18360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4840059
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)esv2258950
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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