A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178749



Internal ID20745789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:15155501..15209400hg38UCSC Ensembl
chr18:15155500..15209399hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3853900
hg1953900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517051
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178749
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00117


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