A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565040



Internal ID20938111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107308275..107309786hg38UCSC Ensembl
chr9:110070556..110072067hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381512
hg191512
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7906n223
Supporting Variantsnssv18279442
Samples
Known GenesRAD23B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565040
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