A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743363



Internal ID20519351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18209143..18209640hg38UCSC Ensembl
chr20:18189787..18190284hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743363
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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