A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092349



Internal ID22001582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43169780..43169780hg38UCSC Ensembl
chr11:43191330..43191330hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092349
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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