A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18014838



Internal ID20581878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86329470..86798786hg38UCSC Ensembl
chr13:86981725..87451041hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38469317
hg19469317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486013
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18014838
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