A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213646



Internal ID20780686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4266111..4275857hg38UCSC Ensembl
chr4:4267838..4277584hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg389747
hg199747
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361314
Supporting Variants
Samples
Known GenesLYAR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213646
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