A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237773



Internal ID20804813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54491318..54492099hg38UCSC Ensembl
chr14:54958036..54958817hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg38782
hg19782
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580397
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237773
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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