A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524869



Internal ID20898230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30515801..30521100hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg385300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202592
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524869
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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