A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5512822



Internal ID289367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86419784..86505976hg38UCSC Ensembl
chr14:86886128..86972320hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3886193
hg1986193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696113
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5512822
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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