A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14375987



Internal ID22311785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122391267..122391340hg38UCSC Ensembl
chr9:125153546..125153619hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3203810
Supporting Variants
SamplesNA19240
Known GenesPTGS1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14375987
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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