A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069878



Internal ID21979111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135452280..135452280hg38UCSC Ensembl
chr7:135137028..135137028hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575441
Samples
Known GenesCNOT4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069878
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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