A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191309



Internal ID20758349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102740311..102745025hg38UCSC Ensembl
chr14:103206648..103211362hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg384715
hg194715
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508961
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191309
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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