A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085828



Internal ID21995061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47456303..47456303hg38UCSC Ensembl
chr15:47748500..47748500hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606286
Samples
Known GenesSEMA6D
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085828
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