A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13679884



Internal ID21201744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40896614..40896614hg38UCSC Ensembl
chr3:40938105..40938105hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2808691
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13679884
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.9375


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