A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525933



Internal ID302080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39042493..39050328hg38UCSC Ensembl
chr19:39533133..39540968hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg387836
hg197836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723306
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525933
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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