A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981162



Internal ID21890505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:143253084..143253488hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17521714
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981162
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