A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734771



Internal ID20510709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:168385493..168385788hg38UCSC Ensembl
chr3:168103281..168103576hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287214
Samples
Known GenesEGFEM1P
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734771
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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