A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3939168



Internal ID21359237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13154460..13154460hg38UCSC Ensembl
chr3:13195960..13195960hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189658
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3939168
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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