A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566933



Internal ID20940004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96653249..96654085hg38UCSC Ensembl
chr9:99415531..99416367hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38837
hg19837
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281571
Samples
Known GenesAAED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566933
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