A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497254



Internal ID20870459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24232510..24233355hg38UCSC Ensembl
chr16:24243831..24244676hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38846
hg19846
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185434
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497254
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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