A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079514



Internal ID21988747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193966247..193966247hg38UCSC Ensembl
chr3:193684036..193684036hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546839
Samples
Known GenesLOC647323
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079514
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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