A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3927527



Internal ID21347596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16498849..16498849hg38UCSC Ensembl
chr20:16479494..16479494hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15186319
SamplesHG002
Known GenesKIF16B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3927527
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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