A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517839



Internal ID20891200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25385714..25395796hg38UCSC Ensembl
chr18:22965678..22975760hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3810083
hg1910083
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178089
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517839
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