A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2341860



Internal ID8012971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:173273246..173273548hg38UCSC Ensembl
Outerchr5:173273040..173273753hg38UCSC Ensembl
Innerchr5:172700249..172700551hg19UCSC Ensembl
Outerchr5:172700043..172700756hg19UCSC Ensembl
Innerchr5:172632855..172633157hg18UCSC Ensembl
Outerchr5:172632649..172633362hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38714
hg19714
hg18714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4812701
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)esv2341860
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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