A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983142



Internal ID56141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41337530..41423369hg38UCSC Ensembl
chr6:41305268..41391107hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3885840
hg1985840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465830
Supporting Variants
Samples
Known GenesNCR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983142
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