A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2414076



Internal ID8085188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:84287343..84287406hg38UCSC Ensembl
Outerchr8:84287167..84287598hg38UCSC Ensembl
Innerchr8:85199578..85199641hg19UCSC Ensembl
Outerchr8:85199402..85199833hg19UCSC Ensembl
Innerchr8:85362133..85362196hg18UCSC Ensembl
Outerchr8:85361957..85362388hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38432
hg19432
hg18432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4556751
SamplesNA18507
Known GenesRALYL
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)esv2414076
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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