A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535652



Internal ID20909010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:46768295..46768904hg38UCSC Ensembl
chr22:47164192..47164801hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38610
hg19610
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205056
Samples
Known GenesTBC1D22A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535652
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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