A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059764



Internal ID21968997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55665426..55665525hg38UCSC Ensembl
chr19:56176792..56176891hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617765
Samples
Known GenesU2AF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059764
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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