A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1607679



Internal ID17307772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:170011944..170011971hg38UCSC Ensembl
Outerchr3:169729732..169729759hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv930484
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformNot reported
CommentsretroCNV insertion of a retrotransposition of C14orf109 mRNA.
ReferenceSchrider_et_al_2013
Pubmed ID23359205
Accession Number(s)nssv1607679
Frequency
Sample Size946
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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