A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561346



Internal ID20934417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94419546..94420231hg38UCSC Ensembl
chr8:95431774..95432459hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279086
Samples
Known GenesRAD54B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561346
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