A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558076



Internal ID331151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58322759..58322810hg38UCSC Ensembl
chr3:58308486..58308537hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16933007
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558076
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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