A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3939219



Internal ID21359288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21046050..21046050hg38UCSC Ensembl
chr20:21026691..21026691hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15188938
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3939219
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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