A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194610



Internal ID20761650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67096713..67097284hg38UCSC Ensembl
chr16:67130616..67131187hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507399
Supporting Variants
Samples
Known GenesCBFB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194610
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