A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390188



Internal ID21381323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:217922895..217923047hg38UCSC Ensembl
chr2:218787618..218787770hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706945
Samples
Known GenesTNS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390188
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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