A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528789



Internal ID304831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36489215..36529071hg38UCSC Ensembl
chr19:36980117..37019973hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3839857
hg1939857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723105
Samples
Known GenesLOC728752, ZNF260, ZNF566
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528789
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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