A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219086



Internal ID20786126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39219695..39220450hg38UCSC Ensembl
chr14:39688899..39689654hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38756
hg19756
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588801
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219086
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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