A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392314



Internal ID21383344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17737062..17737227hg38UCSC Ensembl
chr19:17847871..17848036hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706408
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392314
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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