A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084304



Internal ID21993537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129326283..129326283hg38UCSC Ensembl
chr11:129196178..129196178hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611727
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084304
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