A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368171



Internal ID22593840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109275996..109279084hg38UCSC Ensembl
chr13:109928344..109931432hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg383089
hg193089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932059
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368171
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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