A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553522



Internal ID20926632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:10672801..10695100hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3822300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553522
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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