A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14441693



Internal ID22238045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112024196..112024476hg38UCSC Ensembl
chr11:111894920..111895200hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208439
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14441693
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