A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558164



Internal ID18759240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38898536..38902421hg38UCSC Ensembl
Outerchr22:38897996..38903495hg38UCSC Ensembl
Innerchr22:39294541..39298426hg19UCSC Ensembl
Outerchr22:39294001..39299500hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9756911
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558164
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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