A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552798



Internal ID20925925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50021886..50022479hg38UCSC Ensembl
chr22:50460315..50460908hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205716
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552798
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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