A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706533



Internal ID21378809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34528007..34528339hg38UCSC Ensembl
chr20:33115812..33116144hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392537
Supporting Variants
Samples
Known GenesDYNLRB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706533
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.390805


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