A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553792



Internal ID20926905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42063978..42069545hg38UCSC Ensembl
chr22:42459982..42465549hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg385568
hg195568
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206835
Samples
Known GenesNAGA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553792
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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