A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216207



Internal ID20783247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32657492..32698790hg38UCSC Ensembl
chr5:32657598..32698896hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3841299
hg1941299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6378104
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216207
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