A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1978491



Internal ID7649602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:65575261..65578223hg38UCSC Ensembl
Outerchr1:65575075..65578415hg38UCSC Ensembl
Innerchr1:66040944..66043906hg19UCSC Ensembl
Outerchr1:66040758..66044098hg19UCSC Ensembl
Innerchr1:65813532..65816494hg18UCSC Ensembl
Outerchr1:65813346..65816686hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg383341
hg193341
hg183341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4536103
SamplesNA18507
Known GenesLEPR
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)esv1978491
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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