A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023303



Internal ID83252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70397332..70398715hg38UCSC Ensembl
chr9:73012248..73013631hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg381384
hg191384
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554080
Supporting Variants
Samples
Known GenesKLF9
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023303
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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