A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17609302



Internal ID21801349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24209164..24209164hg38UCSC Ensembl
chr14:24678370..24678370hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085142
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17609302
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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