A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204620



Internal ID20771660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36558108..36583348hg38UCSC Ensembl
chr22:36954155..36979395hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3825241
hg1925241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541839
Supporting Variants
Samples
Known GenesCACNG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204620
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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