A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17613379



Internal ID21805426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69743792..69743792hg38UCSC Ensembl
chr14:70210509..70210509hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088563
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17613379
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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