A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14458105



Internal ID22252036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:876664..880888hg38UCSC Ensembl
chr19:876664..880888hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384225
hg194225
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3195443
Supporting Variants
SamplesHG00733
Known GenesMED16
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14458105
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