A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260799



Internal ID20827839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5163010..5163663hg38UCSC Ensembl
chr3:5204695..5205348hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541422
Supporting Variants
Samples
Known GenesARL8B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260799
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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