A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950154



Internal ID21370223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35226721..35226721hg38UCSC Ensembl
chr20:33814524..33814524hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15186357
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950154
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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