A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264382



Internal ID20831422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169323271..169333178hg38UCSC Ensembl
chr4:170244422..170254329hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg389908
hg199908
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557548
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264382
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00089


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