A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2376333



Internal ID8047444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:13522143..13522232hg38UCSC Ensembl
Outerchr1:13522012..13522371hg38UCSC Ensembl
Innerchr1:13848638..13848727hg19UCSC Ensembl
Outerchr1:13848507..13848866hg19UCSC Ensembl
Innerchr1:13721225..13721314hg18UCSC Ensembl
Outerchr1:13721094..13721453hg18UCSC Ensembl
Cytoband1p36.21
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 Variantsessv4939438
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)esv2376333
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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