A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734293



Internal ID20510228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194025173..194025253hg38UCSC Ensembl
chr3:193742962..193743042hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294927
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734293
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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