A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979855



Internal ID53951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:975434..982778hg38UCSC Ensembl
chr6:975670..983015hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg387345
hg197346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462392
Supporting Variants
Samples
Known GenesLOC285768
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979855
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