A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982794



Internal ID55886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65836663..65836714hg38UCSC Ensembl
chr6:66546556..66546607hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5400912
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982794
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