A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678421



Internal ID21200278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35630256..35630256hg38UCSC Ensembl
chr22:36026303..36026303hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38756
hg19756
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2804201
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678421
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer