A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279478



Internal ID20846518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108945463..108946298hg38UCSC Ensembl
chr9:111707743..111708578hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38836
hg19836
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564664
Supporting Variants
Samples
Known GenesCTNNAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279478
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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