A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14428909



Internal ID22170375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113250305..113251220hg38UCSC Ensembl
chr9:116012585..116013500hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38916
hg19916
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194628
Supporting Variants
SamplesHG00514
Known GenesSLC31A1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14428909
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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