A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584016



Internal ID21532549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14308649..14308732hg38UCSC Ensembl
chr5:14308758..14308841hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126505
SamplesNA19239
Known GenesTRIO
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584016
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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