A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2334135



Internal ID7658560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26885816..26885858hg38UCSC Ensembl
Outerchr4:26885640..26886046hg38UCSC Ensembl
Innerchr4:26887438..26887480hg19UCSC Ensembl
Outerchr4:26887262..26887668hg19UCSC Ensembl
Innerchr4:26496536..26496578hg18UCSC Ensembl
Outerchr4:26496360..26496766hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38407
hg19407
hg18407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4558487
SamplesNA18507
Known GenesSTIM2
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)esv2334135
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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