A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066349



Internal ID21975582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33031585..33031585hg38UCSC Ensembl
chr3:33073077..33073077hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538597
Samples
Known GenesGLB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066349
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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