A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14410208



Internal ID22325119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120442810..120446065hg38UCSC Ensembl
chr3:120161657..120164912hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg383256
hg193256
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3186373
Supporting Variants
SamplesNA19240
Known GenesFSTL1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14410208
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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