A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269049



Internal ID20836089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5351132..5353720hg38UCSC Ensembl
chr5:5351245..5353833hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg382589
hg192589
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574676
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269049
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00059


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