A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546199



Internal ID20919418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48306020..48306121hg38UCSC Ensembl
chr22:48701832..48701933hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205077
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546199
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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