A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951978



Internal ID21372047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134329150..134329150hg38UCSC Ensembl
chr3:134047992..134047992hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189879
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951978
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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