A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1999255



Internal ID7670366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:475558..475876hg38UCSC Ensembl
Outerchr7:475470..475929hg38UCSC Ensembl
Innerchr7:515195..515513hg19UCSC Ensembl
Outerchr7:515107..515566hg19UCSC Ensembl
Innerchr7:481721..482039hg18UCSC Ensembl
Outerchr7:481633..482092hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38460
hg19460
hg18460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4891283
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)esv1999255
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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