A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556659



Internal ID329792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56578293..56578344hg38UCSC Ensembl
chr15:56870491..56870542hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg386019
hg196019
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556659
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer