A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984342



Internal ID21893685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45523590..45523741hg38UCSC Ensembl
chr1:45989262..45989413hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520725
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984342
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