A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521730



Internal ID20895091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5700894..5757778hg38UCSC Ensembl
chr20:5681540..5738424hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3856885
hg1956885
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203902
Samples
Known GenesC20orf196
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521730
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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