A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281578



Internal ID20848618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97379325..97380248hg38UCSC Ensembl
chr9:100141607..100142530hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38924
hg19924
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557712
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281578
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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