A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259828



Internal ID20826868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160046654..160345667hg38UCSC Ensembl
chr3:159764441..160063455hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38299014
hg19299015
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562968
Supporting Variants
Samples
Known GenesC3orf80, IFT80, IL12A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259828
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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