A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701616



Internal ID125282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44553059..44558589hg38UCSC Ensembl
chr15:44845257..44850787hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg385531
hg195531
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556419
Supporting Variants
Samples
Known GenesEIF3J
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701616
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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