A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731702



Internal ID20507623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44047483..44047883hg38UCSC Ensembl
chr20:42676123..42676523hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263497
Samples
Known GenesTOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731702
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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