A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253519



Internal ID20820559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:13904234..13905535hg38UCSC Ensembl
chr20:13884880..13886181hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599892
Supporting Variants
Samples
Known GenesSEL1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253519
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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