A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095680



Internal ID22004913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24848217..24848217hg38UCSC Ensembl
chr15:25093364..25093364hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604498
Samples
Known GenesSNRPN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095680
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