A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865094



Internal ID22640029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87139644..87149531hg38UCSC Ensembl
chr9:89754559..89764446hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg389888
hg199888
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514593
Samples
Known GenesC9orf170
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865094
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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