A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458992



Internal ID237011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32965984..32970797hg38UCSC Ensembl
chr5:32966090..32970903hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg384814
hg194814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16966386
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458992
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