A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1979443



Internal ID7303868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6798574..6798831hg38UCSC Ensembl
Outerchr1:6798482..6798911hg38UCSC Ensembl
Innerchr1:6858634..6858891hg19UCSC Ensembl
Outerchr1:6858542..6858971hg19UCSC Ensembl
Innerchr1:6781221..6781478hg18UCSC Ensembl
Outerchr1:6781129..6781558hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38430
hg19430
hg18430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4873252
SamplesNA18507
Known GenesCAMTA1
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)esv1979443
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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