A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559466



Internal ID332499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30734664..30734715hg38UCSC Ensembl
chr19:31225571..31225622hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg386016
hg196016
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722737
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559466
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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