A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279661



Internal ID20846701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114867939..114868648hg38UCSC Ensembl
chr9:117630219..117630928hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38710
hg19710
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562046
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279661
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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