A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389631



Internal ID21380766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33556219..33556546hg38UCSC Ensembl
chr2:33781286..33781613hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705948
Samples
Known GenesRASGRP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389631
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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