A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9756864



Internal ID18731110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35628103..35630451hg38UCSC Ensembl
Outerchr22:35628091..35630937hg38UCSC Ensembl
Innerchr22:36024150..36026498hg19UCSC Ensembl
Outerchr22:36024138..36026984hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382847
hg192847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558117
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9756864
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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