A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686715



Internal ID110381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32564187..32564256hg38UCSC Ensembl
chr13:33138324..33138393hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506582
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686715
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.014995


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