A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052960



Internal ID21962193
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 StatusM
Merged Variants
Supporting Variantsnssv17626299
Samples
Known GenesIFNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052960
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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