A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279751



Internal ID20846791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121072623..121073705hg38UCSC Ensembl
chr9:123834901..123835983hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg381083
hg191083
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573300
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279751
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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