A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097686



Internal ID22006919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80288306..80288306hg38UCSC Ensembl
chr15:80580648..80580648hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601917
Samples
Known GenesLINC00927
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097686
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