A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405822



Internal ID21063375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:245801..412400hg38UCSC Ensembl
chr6:245801..412400hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38166600
hg19166600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6038n223
Supporting Variantsnssv18232347
Samples
Known GenesDUSP22, IRF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405822
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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