A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766430



Internal ID20542290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42813988..42813988hg38UCSC Ensembl
chr5:42814090..42814090hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265169
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766430
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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