A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2350302



Internal ID8021413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:168538973..168539265hg38UCSC Ensembl
Outerchr2:168538766..168539478hg38UCSC Ensembl
Innerchr2:169395483..169395775hg19UCSC Ensembl
Outerchr2:169395276..169395988hg19UCSC Ensembl
Innerchr2:169103729..169104021hg18UCSC Ensembl
Outerchr2:169103522..169104234hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38713
hg19713
hg18713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4696620
SamplesNA18507
Known GenesCERS6
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)esv2350302
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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