A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524224



Internal ID300433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:222500..246250hg38UCSC Ensembl
chr19:222500..246250hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3823751
hg1923751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17720021
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524224
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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