A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757027



Internal ID18731273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47190289..47192552hg38UCSC Ensembl
Outerchr22:47190234..47192880hg38UCSC Ensembl
Innerchr22:47586039..47588302hg19UCSC Ensembl
Outerchr22:47585984..47588630hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg382647
hg192647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558280
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757027
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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