A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705197



Internal ID128863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98107314..99003177hg38UCSC Ensembl
chr15:98650543..99546406hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38895864
hg19895864
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557763
Supporting Variants
Samples
Known GenesFAM169B, IGF1R, MIR4714, PGPEP1L
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705197
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.038714


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