A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535514



Internal ID311141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131196607..131196607hg38UCSC Ensembl
chr11:131066502..131066502hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17053771
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535514
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