A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391722



Internal ID21382752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18310158..18310621hg38UCSC Ensembl
chr17:18213472..18213935hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706127
Samples
Known GenesTOP3A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391722
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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