A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946507



Internal ID22721998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104319106..104473629hg38UCSC Ensembl
chr14:104785443..104939966hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38154524
hg19154524
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946507
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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