A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278981



Internal ID20488199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190195308..190195621hg38UCSC Ensembl
chr3:189913097..189913410hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746220
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278981
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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