A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662173



Internal ID21610478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79212219..79212219hg38UCSC Ensembl
chr16:79246116..79246116hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg384505
hg194505
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095632
SamplesHG03732
Known GenesWWOX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662173
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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