A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999350



Internal ID21908693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:25656954..25668203hg38UCSC Ensembl
chr5:25657063..25668312hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3811250
hg1911250
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552706
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999350
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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