A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206564



Internal ID22355083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18534546..18534673hg38UCSC Ensembl
chr19:18645356..18645483hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14447990
SamplesHG00733
Known GenesFKBP8
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206564
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