A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739460



Internal ID20515433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193011589..193011853hg38UCSC Ensembl
chr3:192729378..192729642hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283927
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739460
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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