A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440789



Internal ID22106967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34228122..34231419hg38UCSC Ensembl
chr20:32815928..32819225hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg383298
hg193298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15768031
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440789
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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