A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532167



Internal ID308095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:28292812..28297691hg38UCSC Ensembl
chr19:28783719..28788598hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg384880
hg194880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532167
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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