A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526288



Internal ID302423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:826755..837677hg38UCSC Ensembl
chr19:826755..837677hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810923
hg1910923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv235n206
Supporting Variantsnssv17720143
Samples
Known GenesAZU1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526288
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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