A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754557



Internal ID20530417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135452288..135452288hg38UCSC Ensembl
chr7:135137036..135137036hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274982
Samples
Known GenesCNOT4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754557
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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