A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986128



Internal ID58172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:66964993..66965028hg38UCSC Ensembl
chr6:67674886..67674921hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538424
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986128
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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