A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553953



Internal ID20927063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17558792..17582143hg38UCSC Ensembl
chr22:18038493..18064909hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3823352
hg1926417
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204511
Samples
Known GenesSLC25A18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553953
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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