A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281583



Internal ID20848623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97589112..97589302hg38UCSC Ensembl
chr9:100351394..100351584hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558935
Supporting Variants
Samples
Known GenesTMOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281583
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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