A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502536



Internal ID20875782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77687015..77693756hg38UCSC Ensembl
chr15:77979357..77986098hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg386742
hg196742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178026
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502536
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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