A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9756862



Internal ID18731108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35249179..35249964hg38UCSC Ensembl
Outerchr22:35249143..35250163hg38UCSC Ensembl
Innerchr22:35645172..35645957hg19UCSC Ensembl
Outerchr22:35645136..35646156hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381021
hg191021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558115
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9756862
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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