A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268384



Internal ID20835424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43129780..43130256hg38UCSC Ensembl
chr5:43129882..43130358hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563708
Supporting Variants
Samples
Known GenesZNF131
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268384
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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