A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458281



Internal ID236310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121413093..121474455hg38UCSC Ensembl
chr4:122334248..122395610hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3861363
hg1961363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16954560
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458281
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