A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862534



Internal ID22637469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69872882..69880990hg38UCSC Ensembl
chr9:72487798..72495906hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg388109
hg198109
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514176
Samples
Known GenesC9orf135
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862534
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