A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223486



Internal ID20790526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:255301..382600hg38UCSC Ensembl
chr6:255301..382600hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38127300
hg19127300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414891
Supporting Variants
Samples
Known GenesDUSP22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223486
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.64762


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