A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980733



Internal ID54533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21890007..21896461hg38UCSC Ensembl
chr6:21890238..21896692hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386455
hg196455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463190
Supporting Variants
Samples
Known GenesCASC15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980733
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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