A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761994



Internal ID20537854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63351162..63351162hg38UCSC Ensembl
chr20:61982514..61982514hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274236
Samples
Known GenesCHRNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761994
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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