A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274982



Internal ID20484200
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 StatusS
Merged Variantsnsv4754557
Supporting Variants
Samples
Known GenesCNOT4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274982
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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