A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5411426



Internal ID190734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11782404..11782455hg38UCSC Ensembl
chr11:11803951..11804002hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17042846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5411426
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