A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188244



Internal ID20755284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14356680..14390459hg38UCSC Ensembl
chr16:14450537..14484316hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3833780
hg1933780
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497547
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188244
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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