A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193972



Internal ID20761012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50181215..50197377hg38UCSC Ensembl
chr14:50647933..50664095hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3816163
hg1916163
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477187
Supporting Variants
Samples
Known GenesSOS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193972
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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