A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13694189



Internal ID21216038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109489289..109489289hg38UCSC Ensembl
chr13:110141636..110141636hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2792158
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13694189
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