A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281136



Internal ID20848176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80879420..80880274hg38UCSC Ensembl
chr9:83494335..83495189hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562896
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281136
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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