A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212715



Internal ID22359882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:49609111..49638024hg38UCSC Ensembl
Outerchr12:50002894..50031807hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg3828914
hg1928914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14254626
SamplesNA19238
Known GenesFMNL3, PRPF40B
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212715
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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