A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948403



Internal ID21368472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86215788..86215788hg38UCSC Ensembl
chr3:86264938..86264938hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg383656
hg193656
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15188392
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948403
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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