A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276522



Internal ID20485740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128711455..128713927hg38UCSC Ensembl
chr3:128430298..128432770hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg382473
hg192473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735441
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276522
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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