A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14386077



Internal ID22309492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100473048..100473048hg38UCSC Ensembl
chr1:100938604..100938604hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3519697
Supporting Variants
SamplesNA19240
Known GenesCDC14A
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)nssv14386077
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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