A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14404078



Internal ID22299324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35148183..35148183hg38UCSC Ensembl
chr9:35148180..35148180hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3521363
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsInsertion of a AluY mobile element relative to the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14404078
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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