A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281473



Internal ID20848513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93433499..93434629hg38UCSC Ensembl
chr9:96195781..96196911hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381131
hg191131
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563349
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281473
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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