A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543165



Internal ID20916417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26991938..27005049hg38UCSC Ensembl
chr22:27387901..27401012hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3813112
hg1913112
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543165
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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