A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178023



Internal ID20745063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24905378..24911104hg38UCSC Ensembl
chr16:24916699..24922425hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg385727
hg195727
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511283
Supporting Variants
Samples
Known GenesSLC5A11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178023
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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