A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691692



Internal ID115358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67588052..67598470hg38UCSC Ensembl
chr13:68162184..68172602hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3810419
hg1910419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143400
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691692
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00406


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