A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558145



Internal ID18759221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:37348460..37353524hg38UCSC Ensembl
Outerchr22:37347960..37354460hg38UCSC Ensembl
Innerchr22:37744501..37749564hg19UCSC Ensembl
Outerchr22:37744001..37750500hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg386501
hg196500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9756892
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558145
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer