A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989544



Internal ID60454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158964190..158964441hg38UCSC Ensembl
chr6:159385222..159385473hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472373
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989544
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer