A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191877



Internal ID20758917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38988093..39014212hg38UCSC Ensembl
chr18:36568057..36594176hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3826120
hg1926120
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529031
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191877
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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