A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760111



Internal ID20535971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7298857..7298857hg38UCSC Ensembl
chr20:7279504..7279504hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760111
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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