A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254765



Internal ID20821805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39420289..39421159hg38UCSC Ensembl
chr21:40792215..40793085hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595917
Supporting Variants
Samples
Known GenesLCA5L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254765
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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