A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520051



Internal ID20893412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23168388..23181643hg38UCSC Ensembl
chr20:23149025..23162280hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3813256
hg1913256
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203232
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520051
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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