A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280366



Internal ID20847406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:24518327..24546722hg38UCSC Ensembl
chr9:24518325..24546720hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3828396
hg1928396
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560574
Supporting Variants
Samples
Known GenesIZUMO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280366
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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