A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440563



Internal ID22106741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44047485..44047884hg38UCSC Ensembl
chr20:42676125..42676524hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767744
Samples
Known GenesTOX2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440563
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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