A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521922



Internal ID20895283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38760338..38760929hg38UCSC Ensembl
chr20:37388981..37389572hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202249
Samples
Known GenesACTR5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521922
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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