A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691549



Internal ID115215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63399546..63413736hg38UCSC Ensembl
chr13:63973679..63987869hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3814191
hg1914191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500647
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691549
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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