A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2400179



Internal ID8071290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90858884..90859181hg38UCSC Ensembl
Outerchr15:90858676..90859395hg38UCSC Ensembl
Innerchr15:91402114..91402411hg19UCSC Ensembl
Outerchr15:91401906..91402625hg19UCSC Ensembl
Innerchr15:89203118..89203415hg18UCSC Ensembl
Outerchr15:89202910..89203629hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38720
hg19720
hg18720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4952542
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)esv2400179
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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