A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554929



Internal ID328099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93323455..93367118hg38UCSC Ensembl
chr9:96085737..96129400hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3843664
hg1943664
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025697
Samples
Known GenesC9orf129
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554929
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