A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955355



Internal ID37547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128667385..128677475hg38UCSC Ensembl
chr4:129588540..129598630hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3810091
hg1910091
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458921
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955355
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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