A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250350



Internal ID20817390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:230740462..230743201hg38UCSC Ensembl
chr1:230876208..230878947hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg382740
hg192740
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543812
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250350
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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