A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260798



Internal ID20827838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51623902..51624233hg38UCSC Ensembl
chr3:51657918..51658249hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542511
Supporting Variants
Samples
Known GenesRAD54L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260798
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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