A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989545



Internal ID60455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158971707..158973722hg38UCSC Ensembl
chr6:159392739..159394754hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382016
hg192016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464449
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989545
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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