A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753044



Internal ID20528904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79156833..79156833hg38UCSC Ensembl
chr16:79190730..79190730hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288110
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753044
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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