A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215638



Internal ID20782678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:20416701..20447700hg38UCSC Ensembl
chr5:20416810..20447809hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3831000
hg1931000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383419
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215638
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