A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551012



Internal ID20924152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39073511..39084253hg38UCSC Ensembl
chr22:39469516..39480258hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3810743
hg1910743
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204668
Samples
Known GenesAPOBEC3G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551012
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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