A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411993



Internal ID21069546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:253301..458900hg38UCSC Ensembl
chr6:253301..458900hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38205600
hg19205600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6040n223
Supporting Variantsnssv18222579
Samples
Known GenesDUSP22, IRF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411993
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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