A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079046



Internal ID21988279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183697727..183697727hg38UCSC Ensembl
chr3:183415515..183415515hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551319
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079046
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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