A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548684



Internal ID20921867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:46731686..46741107hg38UCSC Ensembl
chr22:47127583..47137004hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg389422
hg199422
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205054
Samples
Known GenesCERK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548684
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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