A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2791347



Internal ID21236685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78879318..78879318hg38UCSC Ensembl
chr11:78590363..78590363hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13684686
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2791347
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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