A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508589



Internal ID20881892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:732016..759219hg38UCSC Ensembl
chr16:782016..809219hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3827204
hg1927204
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179173
Samples
Known GenesNARFL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508589
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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