A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17115758



Internal ID21446105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16498849..16498849hg38UCSC Ensembl
chr20:16479494..16479494hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672087
Supporting Variants
SamplesHG00732
Known GenesKIF16B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17115758
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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