A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206691



Internal ID20773731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21862509..21868609hg38UCSC Ensembl
chr22:22216799..22222899hg19UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg386101
hg196101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535633
Supporting Variants
Samples
Known GenesMAPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206691
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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