A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061068



Internal ID21970301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113947606..113947606hg38UCSC Ensembl
chr4:114868762..114868762hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544768
Samples
Known GenesARSJ
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061068
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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