A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995370



Internal ID21904713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1390820..1390896hg38UCSC Ensembl
chr4:1384608..1384684hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549162
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995370
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