A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2017213



Internal ID7688324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28400645..28402954hg38UCSC Ensembl
Outerchr14:28400454..28403165hg38UCSC Ensembl
Innerchr14:28869851..28872160hg19UCSC Ensembl
Outerchr14:28869660..28872371hg19UCSC Ensembl
Innerchr14:27939602..27941911hg18UCSC Ensembl
Outerchr14:27939411..27942122hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg382712
hg192712
hg182712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4558857
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)esv2017213
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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