A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549289



Internal ID21873644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67339718..67350428hg38UCSC Ensembl
chr4:68205436..68216146hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3810711
hg1910711
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5998309
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549289
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