A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081013



Internal ID21990246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31312692..31312692hg38UCSC Ensembl
chr15:31604895..31604895hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081013
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