A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059720



Internal ID21968953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14615591..14615642hg38UCSC Ensembl
chr19:14726403..14726454hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619809
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059720
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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