A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391216



Internal ID21382246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102813162..102813215hg38UCSC Ensembl
chr14:103279499..103279552hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705842
Samples
Known GenesTRAF3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391216
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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