A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753815



Internal ID20529675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6063345..6063345hg38UCSC Ensembl
chr20:6043991..6043991hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg381253
hg191253
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275968
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753815
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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