A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269919



Internal ID20479137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25102350..25102350hg38UCSC Ensembl
chr14:25571556..25571556hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755726
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269919
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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