A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558224



Internal ID331296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97614272..97614392hg38UCSC Ensembl
chr9:100376554..100376674hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027574
Samples
Known GenesTSTD2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558224
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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