A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223035



Internal ID20790075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63572959..63594671hg38UCSC Ensembl
chr13:64147092..64168804hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3821713
hg1921713
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581788
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223035
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00046


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