A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764639



Internal ID20540499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:57161453..57161453hg38UCSC Ensembl
chr18:54828684..54828684hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273476
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764639
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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