A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv259n206



Internal ID22755563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56327059..56339751hg38UCSC Ensembl
chr19:56838428..56851120hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3812693
hg1912693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5527048, nsv5515314
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv259n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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