A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520495



Internal ID296822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58076110..58079219hg38UCSC Ensembl
chr19:58587478..58590586hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg383110
hg193109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724414
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520495
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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