A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075468



Internal ID21984701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48246425..48246425hg38UCSC Ensembl
chr3:48287915..48287915hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545902
Samples
Known GenesZNF589
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075468
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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