A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626299



Internal ID21818346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39293162..39297609hg38UCSC Ensembl
chr19:39783802..39788249hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg384448
hg194448
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052960
Supporting Variants
Samples
Known GenesIFNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626299
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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