A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268151



Internal ID20477369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34374245..34374245hg38UCSC Ensembl
chr14:34843451..34843451hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752554
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268151
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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