A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14376900



Internal ID22327675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24635007..24635007hg38UCSC Ensembl
chr1:24961498..24961498hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3522504
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsInsertion of a AluS mobile element relative to the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14376900
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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