A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13691406



Internal ID21213257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4138068..4138068hg38UCSC Ensembl
chr11:4159298..4159298hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790027
Supporting Variants
Samples
Known GenesRRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13691406
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.796875


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