A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501720



Internal ID20874957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79912853..79922267hg38UCSC Ensembl
chr16:79946750..79956164hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg389415
hg199415
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501720
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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