A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269078



Internal ID20836118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55055834..55056656hg38UCSC Ensembl
chr5:54351662..54352484hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38823
hg19823
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563149
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269078
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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