A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531027



Internal ID306991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45507059..45507125hg38UCSC Ensembl
chr19:46010317..46010383hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723584
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531027
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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