A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14379071



Internal ID22292626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92496077..92496077hg38UCSC Ensembl
chr12:92889853..92889853hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3524260
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)nssv14379071
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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