A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191696



Internal ID20758736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49906646..49918501hg38UCSC Ensembl
chr14:50373364..50385219hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3811856
hg1911856
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477013
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191696
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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