A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045133



Internal ID21954403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47393254..47398748hg38UCSC Ensembl
chr19:47896511..47902005hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg385495
hg195495
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617925
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045133
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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