A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392782



Internal ID21383812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27599050..27599603hg38UCSC Ensembl
chr22:27995011..27995564hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706672
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392782
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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