A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501469



Internal ID20874703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63013527..63053989hg38UCSC Ensembl
chr16:63047431..63087893hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3840463
hg1940463
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192900
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501469
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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