A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538337



Internal ID20911654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28194464..28212166hg38UCSC Ensembl
chr22:28590452..28608154hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3817703
hg1917703
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4674n223
Supporting Variantsnssv18204961
Samples
Known GenesTTC28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538337
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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