A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983190



Internal ID56174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41985537..41988912hg38UCSC Ensembl
chr6:41953275..41956650hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg383376
hg193376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466802
Supporting Variants
Samples
Known GenesCCND3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983190
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003746


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