A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048284



Internal ID21957517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58586581..58607327hg38UCSC Ensembl
chr19:59097948..59118694hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3820747
hg1920747
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621011
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048284
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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