A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230808



Internal ID20797848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60454875..60456081hg38UCSC Ensembl
chr13:61029009..61030215hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg381207
hg191207
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586282
Supporting Variants
Samples
Known GenesTDRD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230808
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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