A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521725



Internal ID298010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10464060..10464343hg38UCSC Ensembl
chr19:10574736..10575019hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721320
Samples
Known GenesPDE4A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521725
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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