A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280829



Internal ID20490047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172455536..172456930hg38UCSC Ensembl
chr3:172173326..172174720hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg381395
hg191395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738216
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280829
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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