A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254182



Internal ID20821222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17911287..17912305hg38UCSC Ensembl
chr21:19283604..19284622hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381019
hg191019
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597050
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254182
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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