A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558601



Internal ID20931672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:106589801..106592923hg38UCSC Ensembl
chr9:109352082..109355204hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg383123
hg193123
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558601
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