A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14450906



Internal ID22220386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98563070..98569241hg38UCSC Ensembl
chr12:98956848..98963019hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg386172
hg196172
Variant TypeCNV alu deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3179653
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsAbsence of a AluS mobile element insertion that is present in the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14450906
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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