A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059793



Internal ID21969026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40450452..40450522hg38UCSC Ensembl
chr19:40956359..40956429hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622531
Samples
Known GenesBLVRB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059793
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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