A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223059



Internal ID20790099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94731974..94738895hg38UCSC Ensembl
chr10:96491731..96498652hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg386922
hg196922
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593882
Supporting Variants
Samples
Known GenesCYP2C18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223059
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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