A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279342



Internal ID20846382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102661996..102891095hg38UCSC Ensembl
chr9:105424278..105653377hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38229100
hg19229100
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572660
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279342
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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