A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16889803



Internal ID167301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:144966587..146310000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381343414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138813
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16889803
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000469


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