A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586909



Internal ID21535466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:950015..950072hg38UCSC Ensembl
chr19:950015..950072hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106894
SamplesNA19239
Known GenesARID3A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586909
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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