A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979334



Internal ID53595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23351914..23351918hg38UCSC Ensembl
chr6:23352142..23352146hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385
hg195
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560523
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979334
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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