A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989511



Internal ID60430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158704740..158705475hg38UCSC Ensembl
chr6:159125772..159126507hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140473
Supporting Variants
Samples
Known GenesSYTL3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989511
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.167136


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