A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392398



Internal ID21383428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50643371..50643434hg38UCSC Ensembl
chr19:51146628..51146691hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706456
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392398
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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