A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543680



Internal ID20916926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39163363..39165528hg38UCSC Ensembl
chr22:39559368..39561533hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg382166
hg192166
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204673
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543680
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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