A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13693207



Internal ID21215058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34205694..34205694hg38UCSC Ensembl
chr14:34674900..34674900hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794515
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13693207
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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