A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270395



Internal ID20479613
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 StatusS
Merged Variantsnsv4761152
Supporting Variants
Samples
Known GenesFRS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270395
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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