A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266974



Internal ID20834014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69037920..69039131hg38UCSC Ensembl
chr5:68333747..68334958hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg381212
hg191212
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567073
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266974
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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