A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533774



Internal ID20907135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36852998..36913501hg38UCSC Ensembl
chr20:35481401..35541904hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3860504
hg1960504
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202222
Samples
Known GenesSAMHD1, SOGA1, TLDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533774
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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