A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983842



Internal ID21893185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32804645..32804758hg38UCSC Ensembl
chr1:33270246..33270359hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526830
Samples
Known GenesYARS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983842
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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