A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13690433



Internal ID21212287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104300933..104300933hg38UCSC Ensembl
chr14:104767270..104767270hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2793202
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13690433
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.5


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