A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993073



Internal ID21902416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:262071..262204hg38UCSC Ensembl
chr3:303754..303887hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535487
Samples
Known GenesCHL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993073
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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