A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985193



Internal ID21894536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:83732235..83735036hg38UCSC Ensembl
chr1:84197918..84200719hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg382802
hg192802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526659
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985193
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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