A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998179



Internal ID21907522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:80414341..80447421hg38UCSC Ensembl
chr4:81335495..81368575hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3833081
hg1933081
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537611
Samples
Known GenesC4orf22
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998179
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer