A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536229



Internal ID20909582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32515947..32516537hg38UCSC Ensembl
chr22:32911934..32912524hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204564
Samples
Known GenesSYN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536229
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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