A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14429760



Internal ID22171607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13424322..13425732hg38UCSC Ensembl
chr9:13424321..13425731hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg381411
hg191411
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3207222
Supporting Variants
SamplesHG00514
Known GenesFLJ41200
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14429760
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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