A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261244



Internal ID20470462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60274677..60274677hg38UCSC Ensembl
chr14:60741395..60741395hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758355
Supporting Variants
Samples
Known GenesPPM1A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261244
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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