A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2141320



Internal ID7812431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:187845362..187845439hg38UCSC Ensembl
Outerchr3:187845215..187845616hg38UCSC Ensembl
Innerchr3:187563150..187563227hg19UCSC Ensembl
Outerchr3:187563003..187563404hg19UCSC Ensembl
Innerchr3:189045844..189045921hg18UCSC Ensembl
Outerchr3:189045697..189046098hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38402
hg19402
hg18402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4594579
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)esv2141320
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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