A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3930662



Internal ID21350731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171908583..171908583hg38UCSC Ensembl
chr3:171626373..171626373hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15188514
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3930662
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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