A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520789



Internal ID297101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51005511..51007783hg38UCSC Ensembl
chr19:51508767..51511039hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg382273
hg192273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725359
Samples
Known GenesKLK9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520789
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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