A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761424



Internal ID20537284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1853209..1853209hg38UCSC Ensembl
chr4:1854936..1854936hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265655
Samples
Known GenesLETM1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761424
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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