A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561998



Internal ID20935069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114540374..114540979hg38UCSC Ensembl
chr9:117302654..117303259hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279656
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561998
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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