A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070391



Internal ID21979624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42665930..42665930hg38UCSC Ensembl
chr3:42707422..42707422hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553133
Samples
Known GenesZBTB47
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070391
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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