A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17716716



Internal ID140382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24865921..25342639hg38UCSC Ensembl
chr18:22445885..22922603hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38476719
hg19476719
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559964
Supporting Variants
Samples
Known GenesZNF521
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17716716
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.199188


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