A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706529



Internal ID21378805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32231112..32231177hg38UCSC Ensembl
chr20:30818915..30818980hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392533
Supporting Variants
Samples
Known GenesPOFUT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706529
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0431034


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