A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236485



Internal ID20803525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45312294..45312554hg38UCSC Ensembl
chr13:45886429..45886689hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578999
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236485
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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