A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060494



Internal ID21969728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103599283..103599283hg38UCSC Ensembl
chr4:104520440..104520440hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381648
hg191648
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545075
Samples
Known GenesTACR3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060494
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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