A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204995



Internal ID20772035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30659456..30688376hg38UCSC Ensembl
chr22:31055443..31084363hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3828921
hg1928921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549241
Supporting Variants
Samples
Known GenesDUSP18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204995
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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