A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218226



Internal ID20785266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48648541..48651545hg38UCSC Ensembl
chr13:49222677..49225681hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg383005
hg193005
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592485
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218226
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0001


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