A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279298



Internal ID20846338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100155064..100155624hg38UCSC Ensembl
chr9:102917346..102917906hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562750
Supporting Variants
Samples
Known GenesINVS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279298
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00041


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