A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424569



Internal ID203555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154351703..154353929hg38UCSC Ensembl
chr1:154324179..154326405hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382227
hg192227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890367
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424569
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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