A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486918



Internal ID21144471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25058201..25069280hg38UCSC Ensembl
chr13:25632339..25643418hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3811080
hg1911080
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183694
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486918
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