A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678473



Internal ID21200334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100345065..100345065hg38UCSC Ensembl
chr14:100811402..100811402hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2793946
Supporting Variants
Samples
Known GenesWARS
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678473
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.629032


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