A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13691168



Internal ID21213025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90797294..90797294hg38UCSC Ensembl
chr14:91263638..91263638hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2793727
Supporting Variants
Samples
Known GenesTTC7B
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13691168
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.203704


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