A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268036



Internal ID20835076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14631569..14633032hg38UCSC Ensembl
chr5:14631678..14633141hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381464
hg191464
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556070
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268036
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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