A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13697070



Internal ID21218919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113263140..113263140hg38UCSC Ensembl
chr13:113917454..113917454hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381177
hg191177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2793088
Supporting Variants
Samples
Known GenesCUL4A
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13697070
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.828125


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