A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981902



Internal ID21891245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162466128..162466217hg38UCSC Ensembl
chr1:162435918..162436007hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981902
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