A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9756655



Internal ID18384215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:17659166..17661692hg38UCSC Ensembl
Outerchr22:17658735..17662050hg38UCSC Ensembl
Innerchr22:18141932..18144458hg19UCSC Ensembl
Outerchr22:18141501..18144816hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg383316
hg193316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3557908
Supporting Variants
Samples
Known GenesBCL2L13
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9756655
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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