A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2357861



Internal ID8028972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:32109731..32110033hg38UCSC Ensembl
Outerchr17:32109527..32110219hg38UCSC Ensembl
Innerchr17:30436750..30437052hg19UCSC Ensembl
Outerchr17:30436546..30437238hg19UCSC Ensembl
Innerchr17:27460863..27461165hg18UCSC Ensembl
Outerchr17:27460659..27461351hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38693
hg19693
hg18693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4498390
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)esv2357861
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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