A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761152



Internal ID20537012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:69532000..69532000hg38UCSC Ensembl
chr12:69925780..69925780hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270395
Samples
Known GenesFRS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761152
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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