A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5448706



Internal ID226969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:148572059..148575238hg38UCSC Ensembl
chr2:149329628..149332807hg19UCSC Ensembl
Cytoband2q23.1
Allele length
AssemblyAllele length
hg383180
hg193180
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16919076
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5448706
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