A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2404318



Internal ID8075429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:115476009..115476316hg38UCSC Ensembl
Outerchr8:115475794..115476525hg38UCSC Ensembl
Innerchr8:116488236..116488543hg19UCSC Ensembl
Outerchr8:116488021..116488752hg19UCSC Ensembl
Innerchr8:116557412..116557719hg18UCSC Ensembl
Outerchr8:116557197..116557928hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38732
hg19732
hg18732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4945783
SamplesNA18507
Known GenesTRPS1
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)esv2404318
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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