A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263119



Internal ID20830159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13533471..13536386hg38UCSC Ensembl
chr4:13535095..13538010hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382916
hg192916
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574261
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263119
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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