A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461402



Internal ID239356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16218280..16222051hg38UCSC Ensembl
chr6:16218511..16222282hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383772
hg193772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461402
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