A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599359



Internal ID21791404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55811207..55819004hg38UCSC Ensembl
chr14:56277925..56285722hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg387798
hg197798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033171
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599359
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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