A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707920



Internal ID131586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12906887..12907014hg38UCSC Ensembl
chr16:13000744..13000871hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559086
Supporting Variants
Samples
Known GenesSHISA9
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707920
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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