A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980541



Internal ID54408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34687741..34687760hg38UCSC Ensembl
chr6:34655518..34655537hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536382
Supporting Variants
Samples
Known GenesC6orf106
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980541
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.018687


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