A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520358



Internal ID296689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30598218..30613878hg38UCSC Ensembl
chr19:31089125..31104785hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3815661
hg1915661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722726
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520358
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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