A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051731



Internal ID102328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133555206..133555257hg38UCSC Ensembl
chr11:133425101..133425152hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429925
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051731
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008586


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