A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237803



Internal ID20804843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55076532..55078643hg38UCSC Ensembl
chr14:55543250..55545361hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg382112
hg192112
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588313
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237803
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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