A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213266



Internal ID20780306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14663901..14666100hg38UCSC Ensembl
chr5:14664010..14666209hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392019
Supporting Variants
Samples
Known GenesFAM105B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213266
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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