A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989356



Internal ID60328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151466109..151474055hg38UCSC Ensembl
chr6:151787244..151795190hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg387947
hg197947
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467898
Supporting Variants
Samples
Known GenesC6orf211
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989356
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