A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5514899



Internal ID291387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32508043..32528798hg38UCSC Ensembl
chr19:32998949..33019704hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3820756
hg1920756
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722818
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5514899
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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