A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006884



Internal ID20573924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105177121..105177520hg38UCSC Ensembl
chr13:105829472..105829871hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484679
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00097


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