A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746629



Internal ID20522643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39197836..39197895hg38UCSC Ensembl
chr3:39239327..39239386hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288455
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746629
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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