A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237126



Internal ID20804166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58574072..58574888hg38UCSC Ensembl
chr14:59040790..59041606hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594201
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237126
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00289


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