A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520991



Internal ID20894352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24892192..24919831hg38UCSC Ensembl
chr20:24872828..24900467hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3827640
hg1927640
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202549
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520991
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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