A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707921



Internal ID131587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12913126..12913177hg38UCSC Ensembl
chr16:13006983..13007034hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422237
Supporting Variants
Samples
Known GenesSHISA9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707921
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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