A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5408705



Internal ID188029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:243166588..243166591hg38UCSC Ensembl
chr1:243329890..243329893hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16899846
Samples
Known GenesCEP170
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5408705
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