A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14402836



Internal ID22310697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74063728..74063728hg38UCSC Ensembl
chr8:74975963..74975963hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3523740
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)nssv14402836
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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