A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1980460



Internal ID7651572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:148387582..148387661hg38UCSC Ensembl
Outerchr6:148387388..148387853hg38UCSC Ensembl
Innerchr6:148708718..148708797hg19UCSC Ensembl
Outerchr6:148708524..148708989hg19UCSC Ensembl
Innerchr6:148750411..148750490hg18UCSC Ensembl
Outerchr6:148750217..148750682hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38466
hg19466
hg18466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4734030
SamplesNA18507
Known GenesSASH1
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)esv1980460
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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