A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740366



Internal ID20516341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:588436..588601hg38UCSC Ensembl
chr4:582225..582390hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274909
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740366
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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