A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14386169



Internal ID22309372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18942028..18942110hg38UCSC Ensembl
chr9:18942026..18942108hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3203163
Supporting Variants
SamplesNA19240
Known GenesFAM154A
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14386169
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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