A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570852



Internal ID20943923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90456385..90459234hg38UCSC Ensembl
chr9:93218667..93221516hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382850
hg192850
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281389
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570852
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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