A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981171



Internal ID54818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18319500..18321958hg38UCSC Ensembl
chr6:18319731..18322189hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382459
hg192459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469889
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981171
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