A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266667



Internal ID20833707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132993545..132994791hg38UCSC Ensembl
chr5:132329237..132330483hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg381247
hg191247
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572348
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266667
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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