A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584793



Internal ID21533337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43477219..43477822hg38UCSC Ensembl
chr19:43981371..43981974hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105575
SamplesNA19238
Known GenesPHLDB3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584793
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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