A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996071



Internal ID21905414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:179579879..179627636hg38UCSC Ensembl
chr4:180501032..180548789hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3847758
hg1947758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554945
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996071
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