A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686292



Internal ID109958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25029869..25030575hg38UCSC Ensembl
chr13:25604007..25604713hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506109
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686292
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.014518


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