A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082691



Internal ID21991924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85847182..85847182hg38UCSC Ensembl
chr14:86313526..86313526hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602353
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082691
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