A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13684776



Internal ID21206633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27309631..27309631hg38UCSC Ensembl
chr22:27705592..27705592hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2804392
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13684776
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.21875


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