A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3286308



Internal ID22384697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41206..43334hg38UCSC Ensembl
chr12:62406..64534hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg382129
hg192129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1665n152
Supporting Variantsnssv14446658
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences detected as low complexity by RepeatMasker/3.3.0
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3286308
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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