A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5410281



Internal ID189598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28590941..28590992hg38UCSC Ensembl
chr11:28612488..28612539hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044531
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5410281
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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