A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558551



Internal ID20931622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94430343..94431184hg38UCSC Ensembl
chr9:97192625..97193466hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281492
Samples
Known GenesHIATL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558551
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