A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550459



Internal ID20923605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50107237..50155400hg38UCSC Ensembl
chr22:50545666..50593829hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3848164
hg1948164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205719
Samples
Known GenesMOV10L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550459
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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