A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520942



Internal ID20894303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21404463..21477013hg38UCSC Ensembl
chr20:21385101..21457651hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg3872551
hg1972551
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203218
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520942
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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