A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521689



Internal ID20895050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32883101..32888492hg38UCSC Ensembl
chr20:31470907..31476298hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg385392
hg195392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203279
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521689
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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