A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv252n206



Internal ID22755556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44606573..44610217hg38UCSC Ensembl
chr19:45109890..45113535hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg383645
hg193646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5524561, nsv5517131
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv252n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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