A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392854



Internal ID21383884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45423946..45424103hg38UCSC Ensembl
chr22:45819826..45819983hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706707
Samples
Known GenesRIBC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392854
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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