A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14428361



Internal ID22169577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103186412..103186519hg38UCSC Ensembl
chr13:103838762..103838869hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3195514
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14428361
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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