A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059360



Internal ID21968594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204570640..204570640hg38UCSC Ensembl
chr1:204539768..204539768hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg383123
hg193123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059360
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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