A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549241



Internal ID20922409
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 StatusM
Merged Variants
Supporting Variantsnssv18204995
Samples
Known GenesDUSP18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549241
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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