A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14403058



Internal ID22325353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88199974..88211062hg38UCSC Ensembl
chr9:90814889..90825977hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3811089
hg1911089
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197056
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14403058
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