A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18013123



Internal ID20580163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76198475..76198919hg38UCSC Ensembl
chr13:76772611..76773055hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6481916
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18013123
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00056


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