A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038811



Internal ID93618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122529425..122529476hg38UCSC Ensembl
chr10:124288941..124288992hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386015
hg196015
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556387
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038811
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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