A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179966



Internal ID20747006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106532801..106536900hg38UCSC Ensembl
chr13:107185149..107189248hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479713
Supporting Variants
Samples
Known GenesEFNB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179966
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