A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2072312



Internal ID7743423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:70951385..70951785hg38UCSC Ensembl
Innerchr11:70797678..70797742hg19UCSC Ensembl
Outerchr11:70797492..70797929hg19UCSC Ensembl
Innerchr11:70475326..70475390hg18UCSC Ensembl
Outerchr11:70475140..70475577hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38401
hg19438
hg18438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4783551
SamplesNA18507
Known GenesSHANK2
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)esv2072312
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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