A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294389



Internal ID20503607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141665701..141666055hg38UCSC Ensembl
chr3:141384543..141384897hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735219
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294389
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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