A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552914



Internal ID20926032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21626462..21640344hg38UCSC Ensembl
chr22:21980751..21994633hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3813883
hg1913883
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206686
Samples
Known GenesCCDC116, YDJC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552914
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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