A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591582



Internal ID21540158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29566896..29567628hg38UCSC Ensembl
chr19:30057803..30058535hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104256
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591582
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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