A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986641



Internal ID21895984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167937962..167940078hg38UCSC Ensembl
chr2:168794472..168796588hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg382117
hg192117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17521480
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986641
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