A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184391



Internal ID20751431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105134616..105150841hg38UCSC Ensembl
chr13:105786967..105803192hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3816226
hg1916226
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493217
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184391
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer