A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509646



Internal ID286294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89734436..89737424hg38UCSC Ensembl
chr14:90200780..90203768hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg382989
hg192989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509646
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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