A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181973



Internal ID20749013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25710609..25755402hg38UCSC Ensembl
chr14:26179815..26224608hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3844794
hg1944794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477306
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181973
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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