A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17695567



Internal ID119233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109799296..109812459hg38UCSC Ensembl
chr13:110451643..110464806hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3813164
hg1913164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495884
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17695567
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