A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018589



Internal ID21927932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118986509..118989356hg38UCSC Ensembl
chr9:121748787..121751634hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg382848
hg192848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580695
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018589
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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