A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458370



Internal ID236397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:36399484..36439416hg38UCSC Ensembl
chr5:36399586..36439518hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3839933
hg1939933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16963407
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458370
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