A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205240



Internal ID20772280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17697143..17725637hg38UCSC Ensembl
chr20:17677788..17706282hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3828495
hg1928495
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531236
Supporting Variants
Samples
Known GenesBANF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205240
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