A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983624



Internal ID56462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35682056..35682134hg38UCSC Ensembl
chr6:35649833..35649911hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458814
Supporting Variants
Samples
Known GenesFKBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983624
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.112933


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