A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1832n152



Internal ID22817535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46896485..46916160hg38UCSC Ensembl
chr12:47290268..47309943hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg3819676
hg1919676
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3231472, nsv3551470
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
Single strand sequencing, and assortment analysis
PlatformIllumina HiSeq
Strand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv1832n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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