A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081608



Internal ID21990841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97817987..97817987hg38UCSC Ensembl
chr14:98284324..98284324hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614071
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081608
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