A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465733



Internal ID243589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88559922..88564347hg38UCSC Ensembl
chr6:89269641..89274066hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384426
hg194426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986819
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465733
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