A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178551



Internal ID20745591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45055063..45055649hg38UCSC Ensembl
chr14:45524266..45524852hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488497
Supporting Variants
Samples
Known GenesFAM179B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178551
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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