A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13686399



Internal ID21208256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25033666..25033666hg38UCSC Ensembl
chr18:22613630..22613630hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2798416
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13686399
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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