A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9756867



Internal ID18731113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35737587..35738198hg38UCSC Ensembl
Outerchr22:35737455..35738226hg38UCSC Ensembl
Innerchr22:36133634..36134245hg19UCSC Ensembl
Outerchr22:36133502..36134273hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558120
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9756867
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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