A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060614



Internal ID21969847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89594311..89594311hg38UCSC Ensembl
chr3:89643461..89643461hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg381350
hg191350
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556519
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060614
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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