A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18014802



Internal ID20581842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86059734..86062062hg38UCSC Ensembl
chr13:86633869..86636197hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg382329
hg192329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494874
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18014802
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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