A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221310



Internal ID20788350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28168894..28169247hg38UCSC Ensembl
chr13:28743031..28743384hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575783
Supporting Variants
Samples
Known GenesPAN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221310
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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