A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389966



Internal ID21381101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:142677037..142677374hg38UCSC Ensembl
chr2:143434606..143434943hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706821
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389966
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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