A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206688



Internal ID20773728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21721214..21775562hg38UCSC Ensembl
chr22:22075503..22129851hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3854349
hg1954349
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543516
Supporting Variants
Samples
Known GenesMAPK1, YPEL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206688
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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