A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760793



Internal ID20536653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35580695..35580695hg38UCSC Ensembl
chr20:34168617..34168617hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760793
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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