A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530362



Internal ID306349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51213832..51214492hg38UCSC Ensembl
chr19:51717088..51717748hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725374
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530362
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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