A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203406



Internal ID20770446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6210401..6216700hg38UCSC Ensembl
chr20:6191048..6197347hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525585
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203406
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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