A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090884



Internal ID22000117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5247795..5247795hg38UCSC Ensembl
chr11:5269025..5269025hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090884
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