A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279739



Internal ID20846779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120784628..120785305hg38UCSC Ensembl
chr9:123546906..123547583hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558500
Supporting Variants
Samples
Known GenesFBXW2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279739
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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